Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Asymmetric Synthesis by Using the Chirality of l-Ephedrine. III. Reaction of N-(Arylmethylideneamino) ephedrine with Benzylmagnesium Chloride and Phenyllithium
HIROSHI TAKAHASHIHIDEKAZU INAGAKI
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Keywords: phenyllithium
JOURNAL FREE ACCESS

1982 Volume 30 Issue 3 Pages 922-926

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Abstract
Reaction of N-(benzylideneamino) ephedrine (II) with benzylmagnesium chloride gave N-(1, 2-dimethylethylamino) ephedrine (a mixture of III and IV). On the other hand, reaction of N-[(2-phenylethylidene) amino] ephedrine (VII) with phenyllithium gave IV. Hydrogenolysis of these products gave 1, 2-diphenylethylamine with 40% (S) and 91% (R) optical purity, respectively, and l-ephedrine used as a chiral auxiliary reagent was recovered. Reactions of N-(arylmethylideneamino) ephedrines (VIII and IX) with benzylmagnesium chloride gave chiral hydrazines (X and XI), and reactions with phenyllithium gave XII and XIII.
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