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R-(+)硫-代四氢呋喃-2-甲酸的合成
引用本文:孙可一,王平,杨永忠,吴鑫琦,房发俐.R-(+)硫-代四氢呋喃-2-甲酸的合成[J].应用化工,2009,38(12):1824-1825.
作者姓名:孙可一  王平  杨永忠  吴鑫琦  房发俐
作者单位:西安瑞联近代电子材料有限责任公司,陕西,西安,710077
摘    要:以R-(+四)-氢呋喃-2-甲酸为原料,通过草酰氯酰化,与NaHS发生取代反应,合成R-(+)硫-代四氢呋喃-2甲-酸,粗品经柱层析,减压蒸馏纯化。产品收率53.3%,产物结构经MS,1H NMR确认。

关 键 词:R-(+硫)-代四氢呋喃-2-甲酸  R-(+)四-氢呋喃-2甲-酸  法罗培南

The synthesis of R-(+)-thiotetrahydrofuran-2-carboxylic acid
SUN Ke-yi,WANG Ping,YANG Yong-zhong,WU Xin-qi,FANG Fa-li.The synthesis of R-(+)-thiotetrahydrofuran-2-carboxylic acid[J].Applied chemical industry,2009,38(12):1824-1825.
Authors:SUN Ke-yi  WANG Ping  YANG Yong-zhong  WU Xin-qi  FANG Fa-li
Abstract:R-(+)-thiotetrahydrofuran-2-carboxylic acid was synthesized via R-(+)-tetrahydrofuran-2-carboxylic acid by acylation using oxalyl chloride followed by step of substitution reaction using sodium hydrosulfide.The crude product was purified by chromatography column and vacuum distillation.The overall yield was 53.3% and the products was confirmed by MS and ~1H NMR.
Keywords:R-(+)-thiotetrahydrofuran-2-carboxylic acid  R-(+)-tetrahydrofuran-2-carboxylic acid  faropenem
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