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THE PREPARATION METHOD OF (1 R,2S)-(-)-EPHEDRINE OR ITS HYDROCHLORIDE

机译:(1 R,2S)-(-)-哌啶或其盐酸盐的制备方法

摘要

IN this invention, (1 R,2S)-(-)-ephedrine is obtained by reacting, [(S)-(-)-α-methylaminophenylacetone]2 . (2R,3R)-tartaric acid derivatives or the salts of (S)-(-)-α-methylaminophenylacetone and other organic acids with metal borohydride or the mixture consisting of metal borohydride and lewis acid. Since the staring materials don't racemize during the reductive reaction, the ephedrine should be predominant in the product. In addition, the utilization of the metal borohydride is high.
机译:在本发明中,通过使[(S)-(-)-α-甲基氨基苯基丙酮] 2反应,得到(1 R,2S)-(-)-麻黄碱。 (2R,3R)-酒石酸衍生物或(S)-(-)-α-甲基氨基苯基丙酮和其他有机酸与金属硼氢化物或由金属硼氢化物和路易斯酸组成的混合物的盐。由于凝视物质在还原反应过程中不会消旋,因此麻黄碱应在产品中占主导地位。另外,金属硼氢化物的利用率高。

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