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Physical constants and instrumental data (melting point [mp], thin-layer chromatography [TLC] [Rf], gas chromatography [GC] [Rt], [α]D25, 1H- and 13C-nuclear magnetic resonance [NMR], infrared (IR), 70-eV, electron impact-mass spectroscopy [EI-MS], color, and microcrystalline tests) are reported for the individual stereoisomers, racemates, and corresponding hydrochloride salts of 4-methylaminorex (2-amino-4-methyl-5-phenyl-Δ2-oxazoline, 4,5-dihydro-4-methyl-5-phenyl-2-oxazolamine, McN-822, “U4Euh,” “ICE”). The data allow identification and differentiation of illicit samples of 4-methylaminorex.

Methamphetamine, a drug frequently abused in the United States, is often manufactured illicitly. One method commonly employed for this purpose is the Leuckart reaction, which is initiated with methyl benzyl ketone (IV) and either methylamine (I) and formic acid (II) or N-methylformamide (III), producing N-formylmethamphetamine (IX) as an intermediate [1]. Hydrolysis of IX with a strong acid such as hydrochloric acid produces methamphetamine (VI). (See Table 1 for a list of abbreviations and Fig. 1 for corresponding structures.) As the synthesis proceeds, various impurities are accumulated: reactants, byproducts, and intermediates, as well as contaminants arising from within the reagents themselves. The identification of such impurities thus far encountered in this laboratory by gas chromatography/mass spectrometry (GC/MS) and nuclear magnetic resonance (NMR) spectroscopy will be the subject of this discussion.

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