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1-butyryl-4-cinnamylpiperazine AP-237
-
2017-01-30 at 7:03 AM UTCahhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhohhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhhthatexplains everhueeurhuhurhuhttt
but wait who the fuck is 190gt -
2017-01-30 at 8:19 PM UTCIn a 250 mL Parr hydrogenation bottle was placed 0.25g 10% Pd/C
and anhyd NaOAc (1.50 g, 18 mmol). Benzene (50 mL) was added,
followed by acetic anhydride (5mL, 5.41g, 5.32 mmol), and 4 (0.50g,
1.7 mmol). The mixture was shaken under 60 psig of hydrogen for 4 h.
After the uptake of hydrogen had ceased the hydrogenation bottle
was removed from the apparatus, the mixture was diluted with THF
(25 mL), and the catalyst was removed by filtration through a pad
of Celite 545. The catalyst was washed repeatedly with isopropanol
(3 x 50 mL). The washings and mother liquor were collected separately
because of unreacted Ac2O in the filtrate. The mother liquor
was concentrated under vacuum to about one half the original volume,
then toluene (50 mL) was added. The solution was again concentrated
by rotary evaporation. The isopropanol washes were
combined with the residue and also concentrated. The residue was
then dissolved in anhyd MeOH (50 mL). Fumaric acid
(0.198 g, 1.7mmol) was dissolved in MeOH (10 mL) and added to the stirred
methanolic solution of the residue. After stirring for 10 minutes, toluene
(50 mL) was added and the solution was concentrated to dryness
by rotary evaporation. Absolute EtOH was added to the residue
and a white precipitate of 2 fumarate (0.290 g, 0.8 mmol) formed
and was collected by filtration. The filtrate was evaporated and the
residue was dissolved in a minimum amount of MeOH. EtOAc was
added and clear crystals began to form. After storing the solution in
a freezer at –10 °C, 0.170 g of additional product was collected for
a total yield of 0.460 g (74.8%); mp 172–173 °C.
-
2017-01-30 at 11:12 PM UTCThats a garbage synth noob. ^ has nothing to do with anything and is not clandestine. Fuck you.
-
2017-01-31 at 3:22 AM UTC
Originally posted by SCronaldo_J_Trump Thats a garbage synth noob. ^ has nothing to do with anything and is not clandestine. Fuck you.
https://www.erowid.org/archive/rhodium/pdf/nichols/nichols-psilocin.pdf
http://chemistry.mdma.ch/hiveboard/rhodium/equipment/hydrogenation.bomb.html
http://chemistry.mdma.ch/hiveboard/tryptamine/000521336.html
Improvements to the Synthesis of Psilocybin and a Facile Method for
Preparing the O-Acetyl Prodrug of Psilocin
David E. Nichols,* Stewart Frescas
Department of Medicinal Chemistry and Molecular Pharmacology, School of Pharmacy and Pharmacal Sciences, Purdue University, West
Lafayette, Indiana 47907, USA
Fax +1(765)4941414; E-mail drdave@pharmacy.purdue.edu
Received 3 December 1998; revised 11 February 1999
Abstract: An improved procedure to accomplish the O-phosphorylation
of 4-hydroxy-N,N-dimethyltryptamine (psilocin 5) is reported
that utilizes reaction between the O-lithium salt of 5 and tetra-Obenzylpyrophosphate.
The O-benzyl groups were removed by catalytic
hydrogenation over palladium on carbon to afford N,N-dimethyl-4-phosphoryloxytryptamine
(psilocybin, 1). In view of
difficulties encountered in the preparation of 1, it is suggested that
4-acetoxy-N,N-dimethyltryptamine (2) may be a useful alternative
for pharmacological studies. The latter was obtained following catalytic
O-debenzylation of 4-benzyloxy-N,N-dimethyltryptamine in
the presence of acetic anhydride and sodium acetate.
Key words: psilocin, psilocybin, tetra-O-benzylpyrophosphate,
phosphorylation
Recently, several laboratories have initiated clinical studies
of hallucinogenic (psychedelic) agents.1–3
This renewed
interest suggests that there may be some demand
for investigational substances that are suitably pure for
human use that can be prepared in a relatively economical
fashion. Hallucinogens are not commercially available in
large quantities or in purities suitable for human studies,
and research will likely be carried out only with drugs produced
by custom synthesis. Of the various drugs that
might be of interest for this work, most of them, including
mescaline, LSD, DMT, and various substituted amphetamines
are synthesized relatively easily. Indeed, many
hallucinogens are routinely manufactured in clandestine
laboratories.
By contrast, the synthesis of psilocybin, N,N-dimethyl-4-
phosphoryloxytryptamine (1), is more challenging. Nevertheless,
psilocybin has pharmacological features that
make it attractive for clinical research, including a relatively
short duration of action. The increasing worldwide
popularity of psilocybin-containing mushrooms as recreational
drugs also points to the need for more research
with psilocybin.
We re-examined the synthesis of psilocybin reported by
Hofmann and co-workers.4
Although their approach still
remains useful, there were several weak points that could
be addressed to improve the yields and purities of the final
compound.
The overall synthetic route is shown in Scheme 1. The
most troublesome step is the last, the phosphorylation
of psilocin. In the original synthesis by Hofmann et al.,4
the phosphorylation step was accomplished using O,Odibenzylphosphoryl
chloride, an unstable reagent that was
used without purification as a solution in carbon tetrachloride.
Furthermore, the final yield of psilocybin was less
than 20%. In view of the overall difficulty in preparing
this material and its precursors, such a low yield in the last
step was deemed unacceptable.
The present synthesis employs a phosphorylation step using
tetrabenzylpyrophosphate, a stable, crystalline reagent.
The phosphorylation step was complicated by the
previously unreported extremely labile nature of the O,Odibenzyl
ester of psilocybin. Hydrolytic cleavage of one
of the O-benzyl groups occurred rapidly in the presence of
water, at room temperature, and neutral pH. The purification
of the resulting zwitterionic material was much more
complicated than for the basic O,O-dibenzyl material.
Illustrated in Scheme 2 is the facile preparation of 4-acetoxy-DMT5
2. This O-acetyl prodrug of psilocin is much
more easily prepared than psilocybin, and may offer an
economical alternative for clinicians wishing to study the
psychopharmacology of psilocin. This material is readily
crystallized as the fumarate salt, and is considerably more
stable than psilocin itself. It would seem to be an ideal
prodrug to replace psilocybin in future clinical studies,
since psilocin is the principal metabolite of psilocybin.6
The classical Speeter and Anthony synthesis of
tryptamines from indoles served as the precedent for this
work.7
The key reaction of oxalyl chloride with 4-benzyloxyindole
was, however, sluggish. Similarly, the reduction
of the 4-substituted glyoxalylamide 3 was much
slower than for indoles without substitution at this position.
TLC was used to monitor the complete disappearance
of starting material and intermediate reduction
products. The O-benzyl group was then readily removed
by catalytic hydrogenolysis to afford 4-hydroxy-N,Ndimethyltryptamine
(psilocin; 5).
936 D. E. Nichols, S. Frescas PAPER
Synthesis 1999, No. 6, 935–938 ISSN 0039-7881 © Thieme Stuttgart · New York
After experimentation with a variety of phosphorylating
agents, it was finally decided that tetrabenzylpyrophosphate
(TBPP) was the most suitable reagent.8
This crystalline
and stable material is commercially available
(Aldrich), but can also be synthesized readily on a multigram
scale.
The most convenient base for the phosphorylation step
proved to be butyllithium. Generation of the lithium salt
of psilocin in THF at –70 °C, followed by addition of 1.1
equivalents of TBPP, led to the O,O-dibenzyl ester of
psilocybin, with the generation of one equivalent of lithium
O,O-dibenzylphosphate that must ultimately be removed.
While ordinarily removal of the lithium salt
would not be problematic, washing the organic reaction
mixture with water led to unexpected and rapid hydrolysis
of one of the O-benzyl groups. Judicious exclusion of
traces of water allowed the isolation of O,O-dibenzyl ester
that was nearly free of 6. The O,O-dibenzyl intermediate
proved to be so sensitive to water, however, that it was
more practical to use an aqueous workup, allow hydrolysis
to occur, and isolate a product that was largely the
zwitterionic O-monobenzylphosphate 6.
Catalytic hydrogenolysis of the crude O-benzyl ester led
to the formation of psilocybin (1). The procedure was
complicated by small amounts of phosphoric acid generated
from residual dibenzylphosphoric acid carried from
the previous step into the hydrogenolysis reaction. This
highly acidic material leads to discoloration of the product
and prevents satisfactory crystallization. The problem was
solved through the use of anion exchange resin to titrate
the phosphoric acid. The reported pH of a solution of
psilocybin in 50% aqueous ethanol is 5.2.9
Anion exchange
resin (–OH form) was added in portions, with vigorous
and extended stirring, to the enhancemented reaction
solution until the pH of the solution was 5.2. When this
pH was reached, the resin was removed by filtration and
the filtrate was concentrated under vacuum. The crude
product was then recrystallized from a small amount of
methanol, and a large volume of isopropanol, followed by
Scheme 1
Scheme 2
PAPER Improvements to the Synthesis of Psilocybin 937
Synthesis 1999, No. 6, 935–938 ISSN 0039-7881 © Thieme Stuttgart · New York
storage in the freezer. Psilocybin (1) crystallized as long
colorless needles.
As a potential replacement for 1, 4-Acetoxy-N,N-dimethyltryptamine
(2) fumarate was conveniently prepared by
shaking under hydrogen a mixture of 4, acetic anhydride,
and sodium acetate in benzene with Pd/C in a Parr low
pressure hydrogenation apparatus. Following uptake of
the required amount of hydrogen corresponding to O-debenzylation,
the catalyst and insoluble salts were removed
by filtration. One molar equivalent of fumaric acid was
added to the filtrate, and the solution was concentrated to
dryness under vacuum. The resulting solid was recrystallized
to afford white crystals of the desired product. This
material was stable when stored in the cold, but slowly
darkened on storage for several months at ambient temperature.
Mps were determined on a Thomas-Hoover Meltemp melting point
apparatus and are uncorrected except where indicated. 1
H NMR
spectra were recorded on a Bruker ARX 300 MHz spectrometer.
Chemical shifts are reported in d values (ppm) relative to an internal
standard of TMS in CDCl3, except where noted. Abbreviations used
in NMR analysis are as follows: s, singlet; d, doublet; t, triplet; m,
multiplet; br s, broad singlet; dd, doublet of doublets, dt, doublet of
triplets. Microanalyses were obtained from the Purdue Microanalytical
Laboratory. A low pressure Parr apparatus was used for all hydrogenations.
Solvents and reagents were used as purchased, except
as noted. THF was distilled from potassium metal/benzophenone
ketyl. All other compounds were purchased from commercial
sources.
4-Benzyloxyindol-3-yl-N,N-dimethylglyoxylamide (3)
A solution of 4-benzyloxyindole (17.5 g, 0.078 mol) (Biosynth) in
anhyd Et2O (500 mL) was mechanically stirred in a 1 L, 3 necked
flask and cooled in an ice–salt bath to an internal temperature of
0 °C. Oxalyl chloride (20.3 g, 0.16 moles) was added dropwise at a
rate that maintained an internal temperature between 0–5 °C. Stirring
was continued for 3 h at a temperature between 5–10 °C with a
gentle argon sparge to remove evolved HCl. The argon sparge was
replaced by a gas inlet tube and a dry ice/acetone condenser. Anhyd
dimethylamine was then bubbled into the reaction with cooling and
vigorous stirring until a pH (determined by moist pH paper) between
9 and 11 was achieved. At this time, the orange color of the
initial solution had been mostly discharged, and the reaction had the
appearance of a slightly off-white slurry with a few flecks of yellow
unreacted starting material. CH2Cl2 (20 mL) was added to assist solubilization
of the unreacted material and the reaction was stirred for
an additional 6 h to yield finally an off-white slurry. Et2O (150 mL)
was added, and the mixture was cooled to 10 °C. The white solids
were collected by suction filtration on enhancement paper in a Buchner funnel
and then were suspended in distilled H2O (250 mL) and stirred
for 1 h to remove dimethylamine hydrochloride. The slurry was enhancemented,
and the collected solids were washed on the enhancement with distilled
H2O (3 x 75 mL) and hexane (75 mL) and dried overnight in
a vacuum oven. The dried product weighed 18.3 g. The organic filtrates
and washes were combined and the solvent was removed by
rotary evaporation. The residue was dissolved in CH2Cl2 (100 mL)
and the organic solution was washed with distilled H2O (2 x 50 mL)
and brine (2 x 50 mL). After drying (MgSO4) the volume was reduced
by rotary evaporation. The concentrated residual solution
was subjected to flash chromatography over silica gel, first eluting
with CH2Cl2 to recover unreacted indole (1.3 g, 7.4%), followed by
elution with 10% MeOH in CH2Cl2 to recover 3.3 g of 3. The latter
was combined with the initial product to provide a total weight of
21.6 g (85.9%). The crude product was recrystallized from MeOH/
EtOAc to give 19.5 g (77%) of 3 with mp 152–155 °C (Lit.4
mp
146–150 °C).
1
H NMR (300 MHz, CDCl3): d = 2.88, 2.92 (2s, 6H, NCH3), 5.21
(s, 2H, CH2), 6.60 (d, 1H, J =7.92 Hz, Ar), 6.86 (d, 1H, J = 8.04 Hz,
Ar), 7.27–7.37 (m, 3H, Ar), 7.50 (m, 3H, Ar), 10.07 (br s, 1H, NH).
4-Benzyloxy-N,N-dimethyltryptamine (4)
A slurry of LiAlH4 (8.90 g, 0.234 mol) in anhyd THF (100 mL) was
prepared in a 2 L, 3-neck flask, previously dried with a heat gun under
an argon purge. The flask was fitted with a reflux condenser,
mechanical stirrer, and addition funnel. Anhyd dioxane (200 mL)
was added, and the mixture was heated to 60 °C on an oil bath. 4-
benzyloxyindol-3-yl-N,N-dimethylglyoxylamide (3) (14.5 g, 0.045
moles) was dissolved in a mixture of dioxane (250 mL) and THF
(150 mL) and, with rapid stirring, this solution was added dropwise
over 1 h. The oil bath temperature was held at 70 °C for 4 h, followed
by vigorous reflux overnight (16 h) at an oil bath temperature
of 95 °C. Thin layer chromatographic analysis (9:1 CH2Cl2/MeOH;
silica plates) showed nearly complete reduction. The reaction was
heated at reflux for an additional 4 h and then cooled to 20 °C. A
solution of distilled H2O (27 mL) in THF (100 mL) was added
dropwise, resulting in a gray flocculent precipitate. Et2O (250 mL)
was added to assist breakup of the complex and improve filtration.
This slurry was stirred for 1 h and the mixture was then enhancemented with
a Buchner funnel. The enhancement cake was washed on the enhancement with
warm Et2O (2 x 250 mL) and was broken up, transferred back into
the reaction flask and vigorously stirred with additional hot Et2O
(500 mL). This slurry was enhancemented, and the cake was washed on the
enhancement with Et2O (150 mL) and hexane (2 x 150 mL). All of the organic
filtrates were combined and dried (MgSO4). After the drying
agent was removed by filtration, the filtrate was concentrated under
vacuum at 40 °C and dried under high vacuum at 0.01 mm Hg, leading
to crystallization of the residue as a white waxy solid. Recrystallization
from EtOAc yielded 12.57 g, (94.8%) of 4 with mp 124–
126 °C (lit.4
mp 125–126 °C).
1
H NMR (300 MHz, CDCl3): d = 2.14 (s, 6H, NCH3), 2.58 (t, 2H, J
= 8.0 Hz, CH2), 3.04 (t, 2H, J = 8.0 Hz, CH2), 5.17 (s, 2H, CH2),
6.52 (d, 1H, J = 7.6 Hz, Ar), 6.87 (s, 1H, Ar), 6.93 (d, 1H, J = 8.0
Hz, Ar), 7.04 (t, 1H, J = 7.9 Hz, Ar), 7.29–7.39 (m, 3H, Ar), 7.49
(br d, 2H, J = 7.0 Hz, Ar), 8.06 (br s, 1H, NH).
4-Hydroxy-N,N-dimethyltryptamine (Psilocin; 5):
A solution of 4 (4.0 g, 0.0135 moles) in 95% EtOH (250 mL) was
added to 1.5 g Pd/C (10% w/w) in a 500 mL Parr low pressure hydrogenation
bottle. The mixture was shaken under 60 psig of H2
pressure for 2 h. The catalyst was removed by vacuum filtration
through Celite and was washed on the enhancement with EtOH (3 x 50 mL).
The filtrate was concentrated by rotary evaporation. The clear residual
oil was placed under high vacuum and induced to crystallize by
seeding. The white crystalline powder (2.68 g, 97.0%) was used in
the next step without further purification.
1
H NMR (300 MHz, CDCl3): d = 2.36 (s, 6H, NCH3), 2.68 (m, 2H,
CH2),10 2.93 (m, 2H,CH2),10 6.54 (d, 1H, J =7.6, Ar), 6.83 (br d, 2H,
J =12.2 Hz, Ar), 7.03 (t, 1H, J = 7.8 Hz, Ar), 7.86 (br s, 1H, NH),
13.2 (br s, 1H, OH; observed only by integration).
4-O-Monobenzylphosphoryloxy-N,N-dimethyltryptamine (6)
A solution of 0.45 g (2.2 mmol) of psilocin (5) and 0.073 g (0.73
mmol) of diisopropylamine in anhyd THF (50 mL) was magnetically
stirred in a 100 mL 3-necked flask and was cooled to –78 °C in a
dry ice–acetone bath. A 2.5 M solution (1.14 mL, 2.85 mmol) of
BuLi in hexane was added dropwise using a syringe. After complete
addition, the reaction was stirred for 3 min and
tetrabenzylpyrophosphate8
(1.50 g, 2.8 mmol) was added all at
once. The dry ice–acetone bath was replaced by an ice–salt bath,
938 D. E. Nichols, S. Frescas PAPER
Synthesis 1999, No. 6, 935–938 ISSN 0039-7881 © Thieme Stuttgart · New York
and stirring was continued for 1.5 h. TLC (9:1 CHCl3–MeOH; alumina
plates) showed complete disappearance of starting material.
The reaction was quenched by addition of sat. NH4Cl (30 mL). The
biphasic solution was rapidly transferred to a separatory funnel, and
the aqueous layer was separated and washed with EtOAc (2 x 20
mL). The organic layers were combined and washed with brine
(25 mL), followed by drying anhyd (MgSO4). The solution was
then concentrated to a clear residue using rotary evaporation. This
residue (1.12 g) was shown by thin layer chromatography and NMR
analysis to be a mixture of O,O-dibenzylpsilocybin, O-monobenzylpsilocybin
(6), and a small amount of dibenzyl phosphoric acid.
N,N-Dimethyl-4-phosphoryloxtryptamine (Psilocybin; 1)
In a 250 mL Parr hydrogenation bottle was placed 1.0 g of 10% Pd/
C catalyst followed by anhyd MeOH (50 mL). The dibenzyl/
monobenzylphosphoryloxy-N,N-dimethyltryptamine (1.12 g) prepared
in the previous step was added and the mixture was shaken
under 60 psig hydrogen pressure for 3 h, at which time hydrogen uptake
had ceased. The hydrogenation bottle was removed from the
apparatus and the catalyst was removed by filtration through a pad
of Celite 545 on a Buchner funnel. The pH of the clear solution was
measured at 3.7 using a pH meter. Amberlite IRA-400 anion exchange
resin (–OH form) (0.75g) was added in 3 portions to the
well-stirred methanolic solution to raise the pH to 5.3.9
The resin
was removed by vacuum filtration and the resulting clear filtrate
was concentrated to dryness by rotary evaporation. The residue was
dissolved in a minimum amount of hot MeOH, and hot isopropanol
was added to the cloud point. An additional drop of MeOH produced
a clear solution. Upon storage in a –20 °C freezer the product
slowly crystallized as white needles 0.294 g (46.9%, from psilocin).
This product was dried under high vacuum to produce solvent-free
psilocybin, which had mp 212–213 °C (lit.5
mp 210–212 °C).
1
H NMR (300 MHz, D20): d = 2.72 (s, 6H, NCH3), 3.14 (t, 2H, J =
7.3 Hz, CH2), 3.29 (t, 2H, J = 7.5 Hz, CH2), 6.85 (d, 1H, J = 7.6 Hz,
Ar), 6.99 (t, 1H, J = 7.9 Hz, Ar), 7.03 (s, 1H, Ar), 7.09 (d, 1H, J =
8.0 Hz, Ar).
Anal. Calcd for C12H17N2O4P (284.25): C 50.71, H 6.03, N 9.86, P
10.90; found: C 50.37, H 5.91, N 9.68, P 10.75.
4-Acetoxy-N,N-dimethyltryptamine5
fumarate (2)
In a 250 mL Parr hydrogenation bottle was placed 0.25g 10% Pd/C
and anhyd NaOAc (1.50 g, 18 mmol). Benzene (50 mL) was added,
followed by acetic anhydride (5mL, 5.41g, 5.32 mmol), and 4 (0.50g,
1.7 mmol). The mixture was shaken under 60 psig of hydrogen for 4 h.
After the uptake of hydrogen had ceased the hydrogenation bottle
was removed from the apparatus, the mixture was diluted with THF
(25 mL), and the catalyst was removed by filtration through a pad
of Celite 545. The catalyst was washed repeatedly with isopropanol
(3 x 50 mL). The washings and mother liquor were collected separately
because of unreacted Ac2O in the filtrate. The mother liquor
was concentrated under vacuum to about one half the original volume,
then toluene (50 mL) was added. The solution was again concentrated
by rotary evaporation. The isopropanol washes were
combined with the residue and also concentrated. The residue was
then dissolved in anhyd MeOH (50 mL). Fumaric acid (0.198 g, 1.7
mmol) was dissolved in MeOH (10 mL) and added to the stirred
methanolic solution of the residue. After stirring for 10 minutes, toluene
(50 mL) was added and the solution was concentrated to dryness
by rotary evaporation. Absolute EtOH was added to the residue
and a white precipitate of 2 fumarate (0.290 g, 0.8 mmol) formed
and was collected by filtration. The filtrate was evaporated and the
residue was dissolved in a minimum amount of MeOH. EtOAc was
added and clear crystals began to form. After storing the solution in
a freezer at –10 °C, 0.170 g of additional product was collected for
a total yield of 0.460 g (74.8%); mp 172–173 °C.
1
NMR (300 MHz, D2O) d = 2.29 (s, 3H, CH3), 2.72 (s, 6H, NCH3),
2.98 (t, 2H, J = 7.1 Hz, CH2), 3.32 (t, 2H, J = 7.1 Hz, CH2), 6.49 (s,
1H, CH), 6.72 (d, 1H, J = 7.7, Ar), 7.08 (t, 1H, J = 8.0, Ar), 7.16 (s,
1H, Ar), 7.29 (d, 1H, J = 8.3, Ar).
Anal. Calcd for C18H22N2O6 (362.38): C 59.66, H 6.12, N 7.73;
found C 59.43, H 6.35, N 7.58.
Acknowledgement
This work was supported in part by grants DA02189 and DA08096
from the National Institute on Drug Abuse.
References and Notes
(1) Strassman, R.J.; Qualls, C.R. Arch. Gen. Psych. 1994, 51, 85.
(2) Strassman, R.J.; Qualls, C.R., Uhlenhuth, E.H.; and Kellner,
R. Arch. Gen. Psych. 1994, 51, 98.
(3) Grob, C.S.; McKenna, D.J.; Callaway, J.C.; Brito, G.S.;
Neves, E.S.; Oberlaender, G.; Saide, O.L.; Labigalini, E.;
Tacla, C.; Miranda, C.T.; Strassman, R.J.; Boone, K.B. J.
Nerv. Ment. Dis. 1996, 184, 86.
(4) Hofmann, A.; Heim, R.; Brack, A.; Kobel, H.; Frey, A.; Ott,
H.; Petrzilka, T.; Troxler, F. Helv. Chim. Acta. 1959, 42, 1557.
(5) U.S patent 3,075,992, Jan 29, 1963.
(6) Hasler, F.; Bourquin, D.; Brenneisen, R.; Bar, T.;
Vollenweider, F.X. Pharm. Acta Helv., 1997, 72, 175.
(7) Speeter, M.E.; Anthony, W.C. J. Am. Chem. Soc. 1954, 76,
6208.
(8) Khorana, H.G.; Todd, A.R. J. Chem. Soc. 1953, 2257.
(9) Reported pH of psilocybin solution, see ref. 4.
(10) Migliaccio, G.P.; Shieh, T.L.N.; Byrn, S.R.; Hathaway, B.A.;
and Nichols, D.E. J. Med. Chem. 1981, 24, 206; this reference
reports a computer simulation for the average coupling
constants between the methylene protons as Jab = 2.7 Hz and
Jab’ = 7.4 Hz.
Article Identifier:
1437-210X,E;1999,0,06,0935,0938,ftx,en;C07398SS.pdf -
2017-01-31 at 3:35 AM UTC
Originally posted by snab_snib https://www.erowid.org/archive/rhodium/pdf/nichols/nichols-psilocin.pdf
http://chemistry.mdma.ch/hiveboard/rhodium/equipment/hydrogenation.bomb.html
http://chemistry.mdma.ch/hiveboard/tryptamine/000521336.html
Improvements to the Synthesis of Psilocybin and a Facile Method for
Preparing the O-Acetyl Prodrug of Psilocin
David E. Nichols,* Stewart Frescas
Department of Medicinal Chemistry and Molecular Pharmacology, School of Pharmacy and Pharmacal Sciences, Purdue University, West
Lafayette, Indiana 47907, USA
Fax +1(765)4941414; E-mail drdave@pharmacy.purdue.edu
Received 3 December 1998; revised 11 February 1999
Abstract: An improved procedure to accomplish the O-phosphorylation
of 4-hydroxy-N,N-dimethyltryptamine (psilocin 5) is reported
that utilizes reaction between the O-lithium salt of 5 and tetra-Obenzylpyrophosphate.
The O-benzyl groups were removed by catalytic
hydrogenation over palladium on carbon to afford N,N-dimethyl-4-phosphoryloxytryptamine
(psilocybin, 1). In view of
difficulties encountered in the preparation of 1, it is suggested that
4-acetoxy-N,N-dimethyltryptamine (2) may be a useful alternative
for pharmacological studies. The latter was obtained following catalytic
O-debenzylation of 4-benzyloxy-N,N-dimethyltryptamine in
the presence of acetic anhydride and sodium acetate.
Key words: psilocin, psilocybin, tetra-O-benzylpyrophosphate,
phosphorylation
Recently, several laboratories have initiated clinical studies
of hallucinogenic (psychedelic) agents.1–3
This renewed
interest suggests that there may be some demand
for investigational substances that are suitably pure for
human use that can be prepared in a relatively economical
fashion. Hallucinogens are not commercially available in
large quantities or in purities suitable for human studies,
and research will likely be carried out only with drugs produced
by custom synthesis. Of the various drugs that
might be of interest for this work, most of them, including
mescaline, LSD, DMT, and various substituted amphetamines
are synthesized relatively easily. Indeed, many
hallucinogens are routinely manufactured in clandestine
laboratories.
By contrast, the synthesis of psilocybin, N,N-dimethyl-4-
phosphoryloxytryptamine (1), is more challenging. Nevertheless,
psilocybin has pharmacological features that
make it attractive for clinical research, including a relatively
short duration of action. The increasing worldwide
popularity of psilocybin-containing mushrooms as recreational
drugs also points to the need for more research
with psilocybin.
We re-examined the synthesis of psilocybin reported by
Hofmann and co-workers.4
Although their approach still
remains useful, there were several weak points that could
be addressed to improve the yields and purities of the final
compound.
The overall synthetic route is shown in Scheme 1. The
most troublesome step is the last, the phosphorylation
of psilocin. In the original synthesis by Hofmann et al.,4
the phosphorylation step was accomplished using O,Odibenzylphosphoryl
chloride, an unstable reagent that was
used without purification as a solution in carbon tetrachloride.
Furthermore, the final yield of psilocybin was less
than 20%. In view of the overall difficulty in preparing
this material and its precursors, such a low yield in the last
step was deemed unacceptable.
The present synthesis employs a phosphorylation step using
tetrabenzylpyrophosphate, a stable, crystalline reagent.
The phosphorylation step was complicated by the
previously unreported extremely labile nature of the O,Odibenzyl
ester of psilocybin. Hydrolytic cleavage of one
of the O-benzyl groups occurred rapidly in the presence of
water, at room temperature, and neutral pH. The purification
of the resulting zwitterionic material was much more
complicated than for the basic O,O-dibenzyl material.
Illustrated in Scheme 2 is the facile preparation of 4-acetoxy-DMT5
2. This O-acetyl prodrug of psilocin is much
more easily prepared than psilocybin, and may offer an
economical alternative for clinicians wishing to study the
psychopharmacology of psilocin. This material is readily
crystallized as the fumarate salt, and is considerably more
stable than psilocin itself. It would seem to be an ideal
prodrug to replace psilocybin in future clinical studies,
since psilocin is the principal metabolite of psilocybin.6
The classical Speeter and Anthony synthesis of
tryptamines from indoles served as the precedent for this
work.7
The key reaction of oxalyl chloride with 4-benzyloxyindole
was, however, sluggish. Similarly, the reduction
of the 4-substituted glyoxalylamide 3 was much
slower than for indoles without substitution at this position.
TLC was used to monitor the complete disappearance
of starting material and intermediate reduction
products. The O-benzyl group was then readily removed
by catalytic hydrogenolysis to afford 4-hydroxy-N,Ndimethyltryptamine
(psilocin; 5).
936 D. E. Nichols, S. Frescas PAPER
Synthesis 1999, No. 6, 935–938 ISSN 0039-7881 © Thieme Stuttgart · New York
After experimentation with a variety of phosphorylating
agents, it was finally decided that tetrabenzylpyrophosphate
(TBPP) was the most suitable reagent.8
This crystalline
and stable material is commercially available
(Aldrich), but can also be synthesized readily on a multigram
scale.
The most convenient base for the phosphorylation step
proved to be butyllithium. Generation of the lithium salt
of psilocin in THF at –70 °C, followed by addition of 1.1
equivalents of TBPP, led to the O,O-dibenzyl ester of
psilocybin, with the generation of one equivalent of lithium
O,O-dibenzylphosphate that must ultimately be removed.
While ordinarily removal of the lithium salt
would not be problematic, washing the organic reaction
mixture with water led to unexpected and rapid hydrolysis
of one of the O-benzyl groups. Judicious exclusion of
traces of water allowed the isolation of O,O-dibenzyl ester
that was nearly free of 6. The O,O-dibenzyl intermediate
proved to be so sensitive to water, however, that it was
more practical to use an aqueous workup, allow hydrolysis
to occur, and isolate a product that was largely the
zwitterionic O-monobenzylphosphate 6.
Catalytic hydrogenolysis of the crude O-benzyl ester led
to the formation of psilocybin (1). The procedure was
complicated by small amounts of phosphoric acid generated
from residual dibenzylphosphoric acid carried from
the previous step into the hydrogenolysis reaction. This
highly acidic material leads to discoloration of the product
and prevents satisfactory crystallization. The problem was
solved through the use of anion exchange resin to titrate
the phosphoric acid. The reported pH of a solution of
psilocybin in 50% aqueous ethanol is 5.2.9
Anion exchange
resin (–OH form) was added in portions, with vigorous
and extended stirring, to the enhancemented reaction
solution until the pH of the solution was 5.2. When this
pH was reached, the resin was removed by filtration and
the filtrate was concentrated under vacuum. The crude
product was then recrystallized from a small amount of
methanol, and a large volume of isopropanol, followed by
Scheme 1
Scheme 2
PAPER Improvements to the Synthesis of Psilocybin 937
Synthesis 1999, No. 6, 935–938 ISSN 0039-7881 © Thieme Stuttgart · New York
storage in the freezer. Psilocybin (1) crystallized as long
colorless needles.
As a potential replacement for 1, 4-Acetoxy-N,N-dimethyltryptamine
(2) fumarate was conveniently prepared by
shaking under hydrogen a mixture of 4, acetic anhydride,
and sodium acetate in benzene with Pd/C in a Parr low
pressure hydrogenation apparatus. Following uptake of
the required amount of hydrogen corresponding to O-debenzylation,
the catalyst and insoluble salts were removed
by filtration. One molar equivalent of fumaric acid was
added to the filtrate, and the solution was concentrated to
dryness under vacuum. The resulting solid was recrystallized
to afford white crystals of the desired product. This
material was stable when stored in the cold, but slowly
darkened on storage for several months at ambient temperature.
Mps were determined on a Thomas-Hoover Meltemp melting point
apparatus and are uncorrected except where indicated. 1
H NMR
spectra were recorded on a Bruker ARX 300 MHz spectrometer.
Chemical shifts are reported in d values (ppm) relative to an internal
standard of TMS in CDCl3, except where noted. Abbreviations used
in NMR analysis are as follows: s, singlet; d, doublet; t, triplet; m,
multiplet; br s, broad singlet; dd, doublet of doublets, dt, doublet of
triplets. Microanalyses were obtained from the Purdue Microanalytical
Laboratory. A low pressure Parr apparatus was used for all hydrogenations.
Solvents and reagents were used as purchased, except
as noted. THF was distilled from potassium metal/benzophenone
ketyl. All other compounds were purchased from commercial
sources.
4-Benzyloxyindol-3-yl-N,N-dimethylglyoxylamide (3)
A solution of 4-benzyloxyindole (17.5 g, 0.078 mol) (Biosynth) in
anhyd Et2O (500 mL) was mechanically stirred in a 1 L, 3 necked
flask and cooled in an ice–salt bath to an internal temperature of
0 °C. Oxalyl chloride (20.3 g, 0.16 moles) was added dropwise at a
rate that maintained an internal temperature between 0–5 °C. Stirring
was continued for 3 h at a temperature between 5–10 °C with a
gentle argon sparge to remove evolved HCl. The argon sparge was
replaced by a gas inlet tube and a dry ice/acetone condenser. Anhyd
dimethylamine was then bubbled into the reaction with cooling and
vigorous stirring until a pH (determined by moist pH paper) between
9 and 11 was achieved. At this time, the orange color of the
initial solution had been mostly discharged, and the reaction had the
appearance of a slightly off-white slurry with a few flecks of yellow
unreacted starting material. CH2Cl2 (20 mL) was added to assist solubilization
of the unreacted material and the reaction was stirred for
an additional 6 h to yield finally an off-white slurry. Et2O (150 mL)
was added, and the mixture was cooled to 10 °C. The white solids
were collected by suction filtration on enhancement paper in a Buchner funnel
and then were suspended in distilled H2O (250 mL) and stirred
for 1 h to remove dimethylamine hydrochloride. The slurry was enhancemented,
and the collected solids were washed on the enhancement with distilled
H2O (3 x 75 mL) and hexane (75 mL) and dried overnight in
a vacuum oven. The dried product weighed 18.3 g. The organic filtrates
and washes were combined and the solvent was removed by
rotary evaporation. The residue was dissolved in CH2Cl2 (100 mL)
and the organic solution was washed with distilled H2O (2 x 50 mL)
and brine (2 x 50 mL). After drying (MgSO4) the volume was reduced
by rotary evaporation. The concentrated residual solution
was subjected to flash chromatography over silica gel, first eluting
with CH2Cl2 to recover unreacted indole (1.3 g, 7.4%), followed by
elution with 10% MeOH in CH2Cl2 to recover 3.3 g of 3. The latter
was combined with the initial product to provide a total weight of
21.6 g (85.9%). The crude product was recrystallized from MeOH/
EtOAc to give 19.5 g (77%) of 3 with mp 152–155 °C (Lit.4
mp
146–150 °C).
1
H NMR (300 MHz, CDCl3): d = 2.88, 2.92 (2s, 6H, NCH3), 5.21
(s, 2H, CH2), 6.60 (d, 1H, J =7.92 Hz, Ar), 6.86 (d, 1H, J = 8.04 Hz,
Ar), 7.27–7.37 (m, 3H, Ar), 7.50 (m, 3H, Ar), 10.07 (br s, 1H, NH).
4-Benzyloxy-N,N-dimethyltryptamine (4)
A slurry of LiAlH4 (8.90 g, 0.234 mol) in anhyd THF (100 mL) was
prepared in a 2 L, 3-neck flask, previously dried with a heat gun under
an argon purge. The flask was fitted with a reflux condenser,
mechanical stirrer, and addition funnel. Anhyd dioxane (200 mL)
was added, and the mixture was heated to 60 °C on an oil bath. 4-
benzyloxyindol-3-yl-N,N-dimethylglyoxylamide (3) (14.5 g, 0.045
moles) was dissolved in a mixture of dioxane (250 mL) and THF
(150 mL) and, with rapid stirring, this solution was added dropwise
over 1 h. The oil bath temperature was held at 70 °C for 4 h, followed
by vigorous reflux overnight (16 h) at an oil bath temperature
of 95 °C. Thin layer chromatographic analysis (9:1 CH2Cl2/MeOH;
silica plates) showed nearly complete reduction. The reaction was
heated at reflux for an additional 4 h and then cooled to 20 °C. A
solution of distilled H2O (27 mL) in THF (100 mL) was added
dropwise, resulting in a gray flocculent precipitate. Et2O (250 mL)
was added to assist breakup of the complex and improve filtration.
This slurry was stirred for 1 h and the mixture was then enhancemented with
a Buchner funnel. The enhancement cake was washed on the enhancement with
warm Et2O (2 x 250 mL) and was broken up, transferred back into
the reaction flask and vigorously stirred with additional hot Et2O
(500 mL). This slurry was enhancemented, and the cake was washed on the
enhancement with Et2O (150 mL) and hexane (2 x 150 mL). All of the organic
filtrates were combined and dried (MgSO4). After the drying
agent was removed by filtration, the filtrate was concentrated under
vacuum at 40 °C and dried under high vacuum at 0.01 mm Hg, leading
to crystallization of the residue as a white waxy solid. Recrystallization
from EtOAc yielded 12.57 g, (94.8%) of 4 with mp 124–
126 °C (lit.4
mp 125–126 °C).
1
H NMR (300 MHz, CDCl3): d = 2.14 (s, 6H, NCH3), 2.58 (t, 2H, J
= 8.0 Hz, CH2), 3.04 (t, 2H, J = 8.0 Hz, CH2), 5.17 (s, 2H, CH2),
6.52 (d, 1H, J = 7.6 Hz, Ar), 6.87 (s, 1H, Ar), 6.93 (d, 1H, J = 8.0
Hz, Ar), 7.04 (t, 1H, J = 7.9 Hz, Ar), 7.29–7.39 (m, 3H, Ar), 7.49
(br d, 2H, J = 7.0 Hz, Ar), 8.06 (br s, 1H, NH).
4-Hydroxy-N,N-dimethyltryptamine (Psilocin; 5):
A solution of 4 (4.0 g, 0.0135 moles) in 95% EtOH (250 mL) was
added to 1.5 g Pd/C (10% w/w) in a 500 mL Parr low pressure hydrogenation
bottle. The mixture was shaken under 60 psig of H2
pressure for 2 h. The catalyst was removed by vacuum filtration
through Celite and was washed on the enhancement with EtOH (3 x 50 mL).
The filtrate was concentrated by rotary evaporation. The clear residual
oil was placed under high vacuum and induced to crystallize by
seeding. The white crystalline powder (2.68 g, 97.0%) was used in
the next step without further purification.
1
H NMR (300 MHz, CDCl3): d = 2.36 (s, 6H, NCH3), 2.68 (m, 2H,
CH2),10 2.93 (m, 2H,CH2),10 6.54 (d, 1H, J =7.6, Ar), 6.83 (br d, 2H,
J =12.2 Hz, Ar), 7.03 (t, 1H, J = 7.8 Hz, Ar), 7.86 (br s, 1H, NH),
13.2 (br s, 1H, OH; observed only by integration).
4-O-Monobenzylphosphoryloxy-N,N-dimethyltryptamine (6)
A solution of 0.45 g (2.2 mmol) of psilocin (5) and 0.073 g (0.73
mmol) of diisopropylamine in anhyd THF (50 mL) was magnetically
stirred in a 100 mL 3-necked flask and was cooled to –78 °C in a
dry ice–acetone bath. A 2.5 M solution (1.14 mL, 2.85 mmol) of
BuLi in hexane was added dropwise using a syringe. After complete
addition, the reaction was stirred for 3 min and
tetrabenzylpyrophosphate8
(1.50 g, 2.8 mmol) was added all at
once. The dry ice–acetone bath was replaced by an ice–salt bath,
938 D. E. Nichols, S. Frescas PAPER
Synthesis 1999, No. 6, 935–938 ISSN 0039-7881 © Thieme Stuttgart · New York
and stirring was continued for 1.5 h. TLC (9:1 CHCl3–MeOH; alumina
plates) showed complete disappearance of starting material.
The reaction was quenched by addition of sat. NH4Cl (30 mL). The
biphasic solution was rapidly transferred to a separatory funnel, and
the aqueous layer was separated and washed with EtOAc (2 x 20
mL). The organic layers were combined and washed with brine
(25 mL), followed by drying anhyd (MgSO4). The solution was
then concentrated to a clear residue using rotary evaporation. This
residue (1.12 g) was shown by thin layer chromatography and NMR
analysis to be a mixture of O,O-dibenzylpsilocybin, O-monobenzylpsilocybin
(6), and a small amount of dibenzyl phosphoric acid.
N,N-Dimethyl-4-phosphoryloxtryptamine (Psilocybin; 1)
In a 250 mL Parr hydrogenation bottle was placed 1.0 g of 10% Pd/
C catalyst followed by anhyd MeOH (50 mL). The dibenzyl/
monobenzylphosphoryloxy-N,N-dimethyltryptamine (1.12 g) prepared
in the previous step was added and the mixture was shaken
under 60 psig hydrogen pressure for 3 h, at which time hydrogen uptake
had ceased. The hydrogenation bottle was removed from the
apparatus and the catalyst was removed by filtration through a pad
of Celite 545 on a Buchner funnel. The pH of the clear solution was
measured at 3.7 using a pH meter. Amberlite IRA-400 anion exchange
resin (–OH form) (0.75g) was added in 3 portions to the
well-stirred methanolic solution to raise the pH to 5.3.9
The resin
was removed by vacuum filtration and the resulting clear filtrate
was concentrated to dryness by rotary evaporation. The residue was
dissolved in a minimum amount of hot MeOH, and hot isopropanol
was added to the cloud point. An additional drop of MeOH produced
a clear solution. Upon storage in a –20 °C freezer the product
slowly crystallized as white needles 0.294 g (46.9%, from psilocin).
This product was dried under high vacuum to produce solvent-free
psilocybin, which had mp 212–213 °C (lit.5
mp 210–212 °C).
1
H NMR (300 MHz, D20): d = 2.72 (s, 6H, NCH3), 3.14 (t, 2H, J =
7.3 Hz, CH2), 3.29 (t, 2H, J = 7.5 Hz, CH2), 6.85 (d, 1H, J = 7.6 Hz,
Ar), 6.99 (t, 1H, J = 7.9 Hz, Ar), 7.03 (s, 1H, Ar), 7.09 (d, 1H, J =
8.0 Hz, Ar).
Anal. Calcd for C12H17N2O4P (284.25): C 50.71, H 6.03, N 9.86, P
10.90; found: C 50.37, H 5.91, N 9.68, P 10.75.
4-Acetoxy-N,N-dimethyltryptamine5
fumarate (2)
In a 250 mL Parr hydrogenation bottle was placed 0.25g 10% Pd/C
and anhyd NaOAc (1.50 g, 18 mmol). Benzene (50 mL) was added,
followed by acetic anhydride (5mL, 5.41g, 5.32 mmol), and 4 (0.50g,
1.7 mmol). The mixture was shaken under 60 psig of hydrogen for 4 h.
After the uptake of hydrogen had ceased the hydrogenation bottle
was removed from the apparatus, the mixture was diluted with THF
(25 mL), and the catalyst was removed by filtration through a pad
of Celite 545. The catalyst was washed repeatedly with isopropanol
(3 x 50 mL). The washings and mother liquor were collected separately
because of unreacted Ac2O in the filtrate. The mother liquor
was concentrated under vacuum to about one half the original volume,
then toluene (50 mL) was added. The solution was again concentrated
by rotary evaporation. The isopropanol washes were
combined with the residue and also concentrated. The residue was
then dissolved in anhyd MeOH (50 mL). Fumaric acid (0.198 g, 1.7
mmol) was dissolved in MeOH (10 mL) and added to the stirred
methanolic solution of the residue. After stirring for 10 minutes, toluene
(50 mL) was added and the solution was concentrated to dryness
by rotary evaporation. Absolute EtOH was added to the residue
and a white precipitate of 2 fumarate (0.290 g, 0.8 mmol) formed
and was collected by filtration. The filtrate was evaporated and the
residue was dissolved in a minimum amount of MeOH. EtOAc was
added and clear crystals began to form. After storing the solution in
a freezer at –10 °C, 0.170 g of additional product was collected for
a total yield of 0.460 g (74.8%); mp 172–173 °C.
1
NMR (300 MHz, D2O) d = 2.29 (s, 3H, CH3), 2.72 (s, 6H, NCH3),
2.98 (t, 2H, J = 7.1 Hz, CH2), 3.32 (t, 2H, J = 7.1 Hz, CH2), 6.49 (s,
1H, CH), 6.72 (d, 1H, J = 7.7, Ar), 7.08 (t, 1H, J = 8.0, Ar), 7.16 (s,
1H, Ar), 7.29 (d, 1H, J = 8.3, Ar).
Anal. Calcd for C18H22N2O6 (362.38): C 59.66, H 6.12, N 7.73;
found C 59.43, H 6.35, N 7.58.
Acknowledgement
This work was supported in part by grants DA02189 and DA08096
from the National Institute on Drug Abuse.
References and Notes
(1) Strassman, R.J.; Qualls, C.R. Arch. Gen. Psych. 1994, 51, 85.
(2) Strassman, R.J.; Qualls, C.R., Uhlenhuth, E.H.; and Kellner,
R. Arch. Gen. Psych. 1994, 51, 98.
(3) Grob, C.S.; McKenna, D.J.; Callaway, J.C.; Brito, G.S.;
Neves, E.S.; Oberlaender, G.; Saide, O.L.; Labigalini, E.;
Tacla, C.; Miranda, C.T.; Strassman, R.J.; Boone, K.B. J.
Nerv. Ment. Dis. 1996, 184, 86.
(4) Hofmann, A.; Heim, R.; Brack, A.; Kobel, H.; Frey, A.; Ott,
H.; Petrzilka, T.; Troxler, F. Helv. Chim. Acta. 1959, 42, 1557.
(5) U.S patent 3,075,992, Jan 29, 1963.
(6) Hasler, F.; Bourquin, D.; Brenneisen, R.; Bar, T.;
Vollenweider, F.X. Pharm. Acta Helv., 1997, 72, 175.
(7) Speeter, M.E.; Anthony, W.C. J. Am. Chem. Soc. 1954, 76,
6208.
(8) Khorana, H.G.; Todd, A.R. J. Chem. Soc. 1953, 2257.
(9) Reported pH of psilocybin solution, see ref. 4.
(10) Migliaccio, G.P.; Shieh, T.L.N.; Byrn, S.R.; Hathaway, B.A.;
and Nichols, D.E. J. Med. Chem. 1981, 24, 206; this reference
reports a computer simulation for the average coupling
constants between the methylene protons as Jab = 2.7 Hz and
Jab’ = 7.4 Hz.
Article Identifier:
1437-210X,E;1999,0,06,0935,0938,ftx,en;C07398SS.pdf
kill yourself lmaoThe following users say it would be alright if the author of this post didn't die in a fire! -
2017-01-31 at 3:36 AM UTCthe fuck that has to do with opiates fag
-
2017-01-31 at 3:47 AM UTC
Originally posted by SCronaldo_J_Trump the fuck that has to do with opiates fag
opiates are gay, see through the placebo of tolerance and do second-psychadelics. succumb to the true addiction. -
2017-01-31 at 10:16 AM UTC
Originally posted by snab_snib opiates are gay, see through the placebo of tolerance and do second-psychadelics. succumb to the true addiction.
Troll blowing its cover. Nice try. -
2017-01-31 at 1:54 PM UTCIf your gonna post about psychedelics post the complete synthesis and not this spam garbage faggot
-
2017-01-31 at 7:52 PM UTC
Originally posted by Horatio Abernathy Troll blowing its cover. Nice try.
go back to facebook
Originally posted by SCronaldo_J_Trump If your gonna post about psychedelics post the complete synthesis and not this spam garbage faggot
it's not my fault you can't make mushrooms -
2017-01-31 at 7:58 PM UTC
Originally posted by greenplastic I'm also very frugal when it comes to drugs. Although I've been sober for a couple weeks now, I was eating $2 worth of a jumbo sized edible daily to get blazed as fuck. Me and my friend also binged on stimulants all last summer but he went through 9 grand of coke and I went through like $100 of 4f-mph, which is better than coke anyways. If I remember correctly 1 lb of unwashed poppy seeds should have about 100-400 mg morphine in them, and even at the low end, $6 for 100 mg is a steal. I should make a blog about frugally doing drugs.
PM me your most jedi ways of getting high, i lost my job recently -
2017-01-31 at 8:01 PM UTCI can grow shrooms fine I'm not wasting Acetic Anhydride and PD/C on fucking psilocibin
-
2017-01-31 at 8:02 PM UTC
Originally posted by SCronaldo_J_Trump You're a fucking retard of the highest order. I just posted a clandestine synthesis for an opiate stronger than fentanyl easily made from OTC de worming meds.
Early bird gets the worm :-) the best drugs belong to the fastest.
you didnt post the synthesis part
EDIT: nvm im fucking retarded
EDIT2; wait no im not that was snibsnab not you where the F U C K is the directions
Post last edited by cerakote at 2017-01-31T20:04:46.513854+00:00 -
2017-01-31 at 8:09 PM UTCOink oink I'm guna make a pig sandwich
-
2017-01-31 at 8:31 PM UTC
Originally posted by SCronaldo_J_Trump I can grow shrooms fine I'm not wasting Acetic Anhydride and PD/C on fucking psilocibin
>he doesn't have vinegar, coconuts, and https://www.surepure.com/99.99Percent-pure-Palladium-Rod-2-mm-diameter-x-100-mm-long/p/4274 -
2017-01-31 at 11:22 PM UTCThere are no directions because nobody has ever done this. This is ground breaking research.
Originally posted by snab_snib >he doesn't have vinegar, coconuts, and https://www.surepure.com/99.99Percent-pure-Palladium-Rod-2-mm-diameter-x-100-mm-long/p/4274
Acetic anhydride from vinegar..yeah can you please get the fuck off BLTC forever noob.
Are you seriously proposing I make my own Pd/c from a rod of palladium?. That is some uncle fester tier bullshit. What next? Extracting cyanide from apple seeds so I can make p2p?.
I hope to god you never lay hands on a valuable reagent In your pathetic life. A crack smoking monkey would put it to better use than you in 100 lifetimes, retard. -
2017-01-31 at 11:55 PM UTC
Originally posted by SCronaldo_J_Trump Acetic anhydride from vinegar..yeah can you please get the fuck off BLTC forever noob. \
are you implying that it's 'difficult'? or just time consuming?
Originally posted by SCronaldo_J_Trump Are you seriously proposing I make my own Pd/c from a rod of palladium?. That is some uncle fester tier bullshit.
it's the cheapest way of going about it, yes. coconuts provide the best coal.
and your attitude should be elemental and up. if you like freedom.
-
2017-02-01 at 12:01 AM UTCA coppertube of about 70cm length and about 3mm inner diameter is connected to a vessel/flask where acetone is brought into a gaseous state of matter (aka boiling). A batwing propane-burner is installed under the part of the tube at the outlet side which heats the tube to a dull red glow. (The burner is positioned at about 50cm from the tubes inlet). The outlet of the tube leads straight into a big vessel with vinegar. This vessel should be halfway filled with broken glass and be hold at a temperature of about 70°C. The vessel has to be closed except for an outlet connected to an smoothly running aspirator.
The acetone is brought to an straight boil and the tube is purged by the acetone. The burner is started and soon after the tube reached a dull red heat direct over the burners flame ketene will be formed by thermal decomposition of the acetone. The ketene reacts with the acetic acid in the vinegar to form acetic anhydride which reacts with the water to form acetic acid. It is possible to use straight water from start instead of vinegar but this is unfavorable as the reaction of water and ketene is rather slow and ketene would escape. Ketene is poisonous so the aspirator which must run down the drain - no aspirator-station like design here.
After some time you will have a mixture of GAA and acetic anhydride which can be separated by simple distillation. The GAA will be absolute anhydrous. The ridiculous acetic anhydride may be converted to GAA by the addition of water. This should be done ASAP as acetic anhydride is a scheduled compound and might cause legal trouble.
This is a little bit a piggy-setup as the unreacted acetone is washed down the drain and not recovered. But it spares all these washbottles and scrubbers and condensors and stuff, and acetone is asscheap and not regarded enviromental dangerous. (at least the bottles I buy carry no such warning)
Yields: At least 50% from theory, up to 80% with some finetuning.
Post last edited by snab_snib at 2017-02-01T00:03:52.320582+00:00 -
2017-02-01 at 12:07 AM UTCI'm implying that it's fucking retarded when you can order 100ml off ebay with no questions asked.
People that aren't stupid usually make it from methyl iodide. You should try it sometime without a respirator. -
2017-02-01 at 12:11 AM UTCWord of the wise - Avoid any "synthesis" that includes the following terms:
"Broken Glass"
"Dull Red Glow"
"Down the Drain"
yeah you go to so much lengths to avoid breaking the law making a scheduled compounds (which it's not) and you dump your waste products into the municipal water supply breaking several EPA laws, You must have put a lot of thought into this.
