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催化合成肉桂酸异戊酯
引用本文:彭建兵,银董红. 催化合成肉桂酸异戊酯[J]. 精细化工中间体, 2002, 32(6): 25-26
作者姓名:彭建兵  银董红
作者单位:1. 湖南娄底师范高等专科学校化生系,湖南,娄底,417000
2. 湖南师范大学精细催化合成研究所,湖南,长沙,410081
基金项目:湖南省自然科学基金资助项目 (0 1JJY3 0 0 8)
摘    要:以苯甲醛为起始原料 ,经Perkin反应首先制备肉桂酸 ,然后在不同催化剂作用下经酯化反应合成了肉桂酸异戊酯 ,确定了最佳反应物的配料比、催化剂用量等反应条件 ,当对甲苯磺酸的用量为反应体系量的 3% ,酸醇比为 1∶1 3(mol)时 ,可得到 81%的肉桂酸异戊酯 ,并对合成产物的红外光谱和物理常数进行了测定 ,与文献值相符。

关 键 词:对甲苯磺酸  肉桂酸  异戊醇  催化合成  肉桂酸异戊酯
文章编号:1009-9212(2002)06-0025-02
修稿时间:2002-08-16

Catalytic Synthesis of Isoamyl Cinnamate
PENG Jian-hing,et al.. Catalytic Synthesis of Isoamyl Cinnamate[J]. Fine Chemical Intermediates, 2002, 32(6): 25-26
Authors:PENG Jian-hing  et al.
Abstract:The catalytic synthesis of isoamyl cinnamate by the esterifi-cation reaction of cinnamate acid and isoamylol in the presence of different acid catalysts was investigated in this paper. It was found that p-toluenesulfonic (PTS) acid was the efficient catalyst , and also the optimum conditions have been established from the ratio of reactants and the amount of catalyst used in the reaction. The yield of isoamyl cinnamate is 81% when the ratio of cinnamate acid and isoamylol was 1:1. 3, over 3% PTS catalyst. The synthetic isoamyl cinnamate was identified by IR spectrum and its physico-chemical constant, which was in agreement with the authentic sample.
Keywords:phenyl-propenoate  isoamylol  isoamyl 3-phenyl-propenoate  p-toluenesulfonic  catalytic synthesis
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