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#79 F-2
2-M; 6-(2-AMINOPROPYL)-5-METHOXY-2-METHYL-2,3-DIHYDROBENZOFURAN
SYNTHESIS: To a
solution of 43.2 g KOH pellets in 250 boiling
EtOH
there was added 96 g
4-methoxyphenol followed by the slow addition of
131.2 g allyl
bromide, and the mixture was held under refluxing
conditions for 16 h. After cooling, the reaction was added to 1.6 L
H2O, and made strongly basic with 25%
NaOH. This was extracted with
3x100 mL
CH2Cl2, the extracts pooled, washed once with dilute
NaOH and
then once with dilute HCl. Removal of the
solvent under vacuum gave
93.8 g of 4-
allyloxyanisole as a pale amber oil, which was used in the
following reaction without further purification.
A round-bottomed flask containing 93 g crude 4-
allyloxyanisole was
equipped with an immersed thermometer and heated with an external
flame until an exothermic reaction set in at 230 °C. The tem
perature
rose to 270 °C and it was maintained there with the flame for five
minutes. After cooling to room tem
perature, the reaction mix was
poured into 2 L H2O and made strongly basic with the addition of 25%
NaOH. This dark aqueous
phase was washed with 2x200 mL
CH2Cl2, and
then acidified with HCl. This was then extracted with 2x200 mL
CH2Cl2, and the pooled extracts washed first with saturated
NaHCO3 and
then with H2O. Removal of the
solvent under vacuum gave 65.6 g of
2-allyl-4-methoxyphenol as a clear, amber oil. To a
solution of 1.66
g of this crude
phenol in 5 mL hexane with just enough
CH2Cl2 added to
effect a clear
solution, there was added 1.3 g
phenyl isocyanate
followed with three drops of
triethylamine. An exothermic reaction
ensued which spontaneously
deposited white
crystals. These was
removed and hexane washed to give
2-allyl-4-methoxyphenyl N-phenyl
carbamate, with a mp of 88-89 °C. The
acetate ester, from the
phenol
and acetic
anhydride in
pyridine, did not
crystallize.
To a
solution of 37.7 g
2-allyl-4-methoxyphenol in 125 mL glacial
acetic acid there was added 19 g
zinc chloride followed with 63 mL
concentrated HCl. The mixture was held at reflux tem
perature for 40
min, then cooled to room tem
perature, diluted with 300 mL H2O, and
extracted with 2x200 mL
CH2Cl2. The pooled extracts were washed
repeatedly with 8%
NaOH until the washings remained basic. Removal of
the
solvent under vacuum gave a clear pale yellow oil that was
distilled at the water pump. A fraction boiling at 150-165 °C was
5-methoxy-2-methyl-2,3-dihydrobenzofuran which weighed 25 g and which
was a highly refractive colorless oil. The infra-red
spectrum
indicated that some small amount of hydroxy group was present, but the
NMR spectrum was in complete accord with the
benzofuran structure. A
higher cut in this
distillation gave 4.5 g of a
phenolic product
tentatively assigned the structure of
4-methoxy-2-propenylphenol. The
target
dihydrobenzo-furan has also been
synthesized from the open-ring
o-allyl
phenol in acetic acid
solution with the addition of a
catalytic amount of concentrated H2SO4.
To a half-hour pre-incubated mixture of 69 g POCl3 and 60 g
N-
methylformanilide there was added 29.0 g
5-methoxy-2-methyl-2,3-dihydrobenzofuran and the mixture was heated on
the steam bath for 2 h. The reaction mixture was poured into 1 L H2O,
and allowed to stir overnight. The brown gummy solids were removed by
filtration, and air dried as completely as possible. These weighed 32
g and were shown by GC on OV-17 to consist of two
benzaldehyde isomers
in a ratio of 7:2. This was triturated under 18 mL MeOH, and the
un
dissolved solids removed by filtration and washed with 6 mL
additional MeOH. The mother liquor and washings were saved. The 17.8
g of dull yellow solids that were obtained were repeatedly extracted
with 75 mL portions of boiling hexane (4 extracts were required) and
each extract, on cooling,
deposited yellow
crystals of the major
aldehyde. The dried
crystals of
6-formyl-5-methoxy-2-methyl-2,3-dihydrobenzofuran were combined (9.5
g) and had a mp of 80-82 °C. The
methanol washes saved from above
were stripped of
solvent, and the sticky, orange solids that remained
were enriched in the minor
aldehyde isomer (3:2 ratio). Several
injections of this crude material into a preparative GC OV-17 column
gave sufficient quantities of the "wrong"
isomer for
NMR
characterization. The
2-methyl group was intact (eliminating the
possibility of a
dihydrobenzopyran isomer) and the ring meta-proton
splitting required that the
formyl group be in the
benzofuran
7-position. This
crystalline solid was, therefore,
7-formyl-5-methoxy-2-methyl-2,3-dihydrobenzofuran.
A
solution of 9 g of
6-formyl-5-methoxy-2-methyl-2,3-dihydrobenzofuran
in 35 mL glacial acetic acid was treated with 6 mL of
nitroethane
followed with 3.1 g
anhydrous ammonium acetate. This mixture was
heated on the steam bath for 4 h, diluted with half its volume with
warm H2O, and seeded with a bit of product that had been obtained
separately. The slightly turbid
solution slowly
crystallized as it
cooled, and was finally held at 0 °C for several h. The deep orange
product was removed by filtration, washed with 50% acetic acid, and
air dried to constant weight. There was thus obtained 7.0 g
5-methoxy-2-methyl-6-(2-nitro-1-propenyl)-2,3-dihydrobenzofuran with a
mp of 89-90 °C from MeOH.
A suspension of 5.0 g LAH in 500 mL of well stirred
anhydrous Et2O at
a gentle reflux, was treated with a warm, saturated
solution of 7.0 g
5-methoxy-2-methyl-6-(2-nitro-1-propenyl)-2,3-dihydrobenzofuran in
Et2O added dropwise. The mixture was kept at reflux tem
perature for
36 h, allowed to stand 2 days, and then the excess
hydride destroyed
by the cautious addition of 500 mL 6% H2SO4. The
phases were
separated, and the aqueous
phase washed with 2x200 mL
CH2Cl2. A total
of 125 g
potassium sodium tartrate was added to the aqueous
phase, and
sufficient 25%
NaOH added to bring the
pH to about 10. This
phase was
extracted with 3x150 mL
CH2Cl2, and the pooled extracts were stripped
of
solvent under vacuum. The
residual oil (4.8 g, amber in color) was
dissolved in 300 mL
anhydrous Et2O which, upon saturation with
anhydrous HCl gas gave a clear
solution that suddenly
deposited white
crystals. The
hydrochloride salt of
6-(2-aminopropyl)-5-methoxy-2-methyl-2,3-dihydrobenzofuran weighed 2.3
g and was not satisfactory as a solid derivative, but it appears that
the oxalate salt is both
nonhygroscopic and quite stable. It (F-2)
had a mp of 216-218 °C and it displayed a textbook
NMR.
DOSAGE: greater than 15 mg.
DURATION: unknown.
EXTENSIONS AND COMMENTARY: This material, which is certainly a mixture
of two
diastereoisomeric pairs of racemates since there are two chiral
centers present, showed no effects at levels of up to 15 milligrams
orally. Doses of 100 mg/Kg were without effects in mice following
i.p. injections, although half again this amount proved to be lethal.
In rats trained to discriminate LSD from
saline, F-2 proved to be
about 40 times less potent than the reference compound DOM, requiring
some 5 mg/Kg for positive responses. But the human trials were only
up to about 0.2 mg/Kg.
This was the prototype compound that was originally put tog
ether to
justify giving a paper at a marijuana conference in Sweden, in 1968.
Although I had never done much with marijuana or with its principal
ingredients, I thought maybe I could bend the topic a bit to embrace
some potentially active
phenethylamines. There is a story of an
international conference held in Geneva a few years earlier to discuss
the worrisome decrease in the elephant population. A German zoologist
invested a full eight-hour day in a summary of his 21 volume treatise
on the anatomy and the
physiology of the elephant. A French
sociologist presented a lively slide show on the mating rituals and
rutting behavior of the elephant. And a rabbi from Tel Aviv entitled
his talk: "Elephants and the Jewish Problem." My Swedish talk should
have been named "
Marijuana and the
Psychedelic Am
phetamines." The
memorable story of meeting the chief of the Swedish
equivalent of the
Bureau of Narcotics, and ending up playing Mozart sonatas in the attic
of his home, has been spun out elsewhere in the book.
The original concept was a grand plan to imitate two of the three
rings of
tetrahydrocannabinol. There is an aromatic ring (with an
alkyl group and two oxygens on it) and it is fused to a pyran ring
with a couple of
methyl groups on it. So, if one were to tie the
methyl group at the 4-position of DOM around with a short
carbon chain
into the oxygen atom at the five position, one could squint and say
that the resulting
amphetamine was kinda something like an
analogue of
THC. Thus, the resulting six-membered ring (a pyran) or five-membered
ring (a furan) could be peppered with
methyl groups at different
locations (and up to two per location). If the ring was a
five-membered structure, then the parent system would be a
benzofuran,
and the location of
methyl groups on the ring would be indicated by
the appropriate numbers following the letter RFS which would stand for
"furan". And if it were to be a six-membered ring, the resulting
benzopyran would be indicated with a RPS for pyran, and again the
methyl group or groups would be indicated by the
substitution
position. This code would cover all
polymethylated homologues with
codes that would look like F-22 and P-2234. If any of them showed up
with fascinating activities, I would extend
methyls to
ethyls, and
work out some whole new naming code at some future time. An early
system, naming this compound 2-M for a
methyl group on the 2-position
of the furan ring, was abandoned when it became apparent that the
pyran world would screw everything up.
The isolation of characterizable quantities of
7-formyl-5-methoxy-2-methyl-2,3-dihydrobenzofuran from the
benzaldehyde recipe above gave a fleeting fantasy of a whole new
direction that this little project might go. If this unexpected
benzaldehyde were to be converted to the corresponding
amphetamine,
one would have
7-(2-aminopropyl)-5-methoxy-2-methyl-2,3-dihydrobenzofuran. Suddenly
here would be a
2,3,5-trisubstituted thing with a ring at the
2,3-position, similar to the still unmade M
MDA-4. The temptation to
be diverted in this way lasted, fortunately, only a few minutes, and
the project was shelved. Someday, when there are buckets of spare
time or hosts of eager graduate students, some fascinating chemistry
might lie this way, and maybe some fascinating
pharmacology, even.
The plain furan
analogue, without any
methyl groups on it, has been
made. Five-
methoxybenzofuran formed the 6-
formyl derivative (the
aldehyde) with a mp of 79-80 °C and from it the
nitrostyrene (orange
needles, mp 89-91 °C) and the final
amphetamine (white solids, as the
methane sulfonate, mp 141-144 °C) were prepared in a manner similar to
the preparation of F-2 above. In the rat studies, it was three times
more potent than F-2, but still some 15 times less potent than DOM.
And in initial human trials (of up to 30 milligrams) there were again
no effects noted. Naming of this material is easy chemically
(
6-(2-aminopropyl)-5-methoxy-2,3-dihydrobenzofuran) but tricky as to
code. If the numbers that follow the RFS give the location of the
methyl groups, then this material, without any such groups, can have
no numbers following, and should properly be simply "F." OK, it is
"F." The preparation or the attempted preparations of other
homologues
such as F-23 and F-233 are outlined under the recipe for F-22.
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