NMR-STUDIES OF DRUGS - ENANTIOMERIC EXCESS DETERMINATION OF N-ACETYLCATHINONE WITH EU(HFC)3

A technique for determination of enantiomeric excess of cathinone, 2-amino-1-phenyl-1-propanone, by use of the chiral lanthanide shift reagent (LSR), tris[3-(heptafluoropropylhydroxymethylene)-d-camphorato]europium(III), Eu(HFC)3, is described. The hydrochloride salt of the cathinone sample is first converted directly to the N-acetyl derivative without need for isolation of the potentially unstable cathinone free base. Addition of Eu(HFC)3 to the crude acetylated cathinone resulted in near-baseline resolution of the CH3CO resonances of the enantiomers. Analytical utility and the sense of magnetic nonequivalence of this signal were demonstrated using "spiked" non-racemic samples.