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(R)4-羟基-2-氧代-1-吡咯烷基乙酰胺的合成
引用本文:陈雪,雷英杰,丁玫,毕野.(R)4-羟基-2-氧代-1-吡咯烷基乙酰胺的合成[J].精细化工中间体,2011,41(5):21-23.
作者姓名:陈雪  雷英杰  丁玫  毕野
作者单位:天津理工大学化学化工学院,天津,300384
基金项目:天津市高等学校科技发展基金资助项目(20080509)
摘    要:以氯乙酰乙酸乙酯为原料,利用生物催化还原反应以及与甘氨酰胺的缩合反应,得到(R)4-羟基-2-氧代-1-吡咯烷基乙酰胺又称(R)-奥拉西坦],探讨了物料比、碱介质和温度对缩合反应的影响,其结构经比旋光度和1H NMR确证,总收率为52.7%。

关 键 词:(R)-奥拉西坦  生物催化还原  合成

Synthesis of(R) 4-Hydroxy-2-oxo-1-pyrrolidineacetamide
CHEN Xue,LEI Ying-jie,DING Mei,RI Ye.Synthesis of(R) 4-Hydroxy-2-oxo-1-pyrrolidineacetamide[J].Fine Chemical Intermediates,2011,41(5):21-23.
Authors:CHEN Xue  LEI Ying-jie  DING Mei  RI Ye
Affiliation:CHEN Xue,LEI Ying-jie,DING Mei,BI Ye(College of Chemistry & Chemical Engineering,Tianjin University of Technology,Tianjin 300384,China)
Abstract:The asymmetric reduction of ethyl 4-chloro-3-oxobutanoate to the title compound(i.e.(R)-oxyracetam)catalyzed by Saccharomyces cerevisiae and followed with the condensation of 2-amino-acetamide in alkaline solution was investigated.The target compound was obtained in 52.7% yield and confirmed by specific rotation and 1H NMR.
Keywords:(R)-oxyracetam  bioreduction  synthesis  
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