SYNTHESIS: To a solution of 45 g 3,4,5trimethoxybenzaldehyde in 1.2 L IPA, there was added 125 g nitropropane and 67.5 g tbutylammonium acetate and the reaction mixture was held at reflux for 16 h. This was poured into 6 L H2O, and extracted with 2×250 mL hexane. The pooled extracts were stripped of solvent under vacuum giving a residue that slowly set to a crystalline mass. On filtering, there was obtained 9.4 g of a crude yellow

product which, on recrystallization from hexane provided 8.7 g of slightly sticky bright yellow crystals of 2-nitro-1-(3,4,5trimethoxyphenyl)butene-1, with a mp of 71-73 °C. A second recrystallization from hexane gave fine yellow crystals with a mp of 72-73 °C. Attempts at the preparation of this nitrostyrene by the more conventional methods with ammonium acetate in acetic acid led either to the formation of a white product C23H30N2O8 which was composed of a molecule of the nitrostyrene, one of the benzaldehyde itself, and a molecule of ammonia, or to 3,4,5trimethoxybenzonitrile, from reaction with the decomposition products of nitropropane.

A stirred suspension of 5.9 g LAH in 310 mL anhydrous Et2O was held at a gentle reflux in an inert atmosphere. A solution of 8.5 g 2-nitro-1-(3,4,5-trimethoxyphenyl)butene-1 in 125 mL Et2O is added drop-wise over the course of 0.5 h. The reaction was maintained at reflux for 6 h, then cooled, and the excess hydride destroyed by the cautious addition of 300 mL 1.8 N H2SO4. The phases were separated, and the aqueous phase brought to a pH of 6 by the addition of a saturated Na2CO3 solution. The neutral solution was brought to a boil, and clarified by filtration through paper. To the hot filtrate there was added a solution of 8.9 g picric acid in 100 mL boiling EtOH. The mixture was stirred and cooled, with the formation of a heavy yellow crystalline mass. After standing in the ice tub for several hours the mixture was filtered, providing 8.0 g of the picrate salt with a mp of 176-181 °C from H2O. A solution of this salt in 300 mL boiling H2O was treated with 60 mL concentrated HCl. On cooling, there was a deposition of picric acid, which was removed by filtration. The aqueous filtrate was washed with 3×50 mL nitrobenzene, then with 3×50 mL Et2O. The pH was brought above 9 by the addition of aqueous NaOH, and the filtrate was extracted with 3×100 mL CH2Cl2. Removal of the solvent from the pooled extracts gave a nearly colorless oil, which was dissolved in 300 mL anhydrous Et2O and saturated with hydrogen chloride gas. The white crystals of 2-amino-1(3,4,5-trimethoxyphenyl)butane hydrochloride (AEM) were removed by filtration, Et2O washed, and air dried. They weighed 4.72 g.

DOSAGE: greater than 220 mg.

DURATION: unknown.

EXTENSIONS AND COMMENTARY: The extension of the two-carbon chain of mescaline by alpha-methylation to the three carbon chain of TMA approximately doubled the potency of the compound. And it was felt to be a completely logical possibility that, by extending it one more carbon atom, to the four carbon chain of alpha-ethyl-mescaline, it might double again. And following that logical progression, the doubling of potency with each additional carbon atom, the factor would be 2 to the 7th power by the alpha-octyl (or 256x that of mescaline, or a milligram as active dose) and with a side chain of a 70-carbon alkyl group (alpha-heptacontylmescaline) it would take just a single molecule to be intoxicating. This was rich fantasy stuff. As an active compound, just where would it go in the brain? With an 80-carbon side-chain, would onethousandth of a single molecule be enough for a person? Or might a single molecule intoxicate a thousand people? And how long a chain on the alpha-position might be sufficient that, by merely writing down the structure on a piece of paper, you would get high? Maybe just conceiving the structure in your mind would do it. That is, after all, the way of homeopathy.

Maybe it was just as well that this added two-carbon side-chain with lowered activity was already enough to disprove the doubling pattern. But by the time this non-activity had been learned, the alpha series had already been pushed out quite aways. The machinery of making the appropriate nitroalkane was straightforward, by reaction of the alkyl halide with nitrous acid, and separating the unwanted nitrite ester from the wanted nitroalkane by fractional distillation. The nitrostyrenes all formed reasonably although often in terrible yields, and reduced reasonably, and all formed crystalline picrates for isolation and crystalline hydrochloride salts for pharmacological manipulation. But since the first of these, AEM, was not active, there was no enthusiasm for tasting anything higher. This family was never published; why publish presumably inactive and thus uninteresting material? The Table presents the properties of the precursor nitrostyrenes, and the product picrate and hydrochloride salts, at least whatever information I can still find after thirty years:

TABLE. Physical Properties of the a-Alkylmescaline Homologues and their Precursor Nitrostyrenes

Code, Name, NS mp deg C, picrate mp deg C, HCl mp deg C

  • APM  Alpha-propylmescaline 82-83,   214-218
  • ABM  Alpha-butylmescaline 73-74,   169-174 182-184
  • AAM  Alpha-amylmescaline 54-55,   162-163 155-158
  • AHM  Alpha-hexylmescaline 51-52
  • ASM  Alpha-heptylmescaline 43-44
  • AOM  Alpha-octylmescaline
  • ANM  Alpha-nonylmescaline 46-47
  • AUM  Alpha-undecylmescaline **
  • ASM  Alpha-heptylmescaline 43-44
  • AOM  Alpha-octylmescaline
  • ANM  Alpha-nonylmescaline 46-47
  • AUM  Alpha-undecylmescaline ***

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