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依帕司他中间体α-甲基肉桂醛的合成
引用本文:左华,赵宝祥,王大威.依帕司他中间体α-甲基肉桂醛的合成[J].精细化工中间体,2003,33(6):36-37.
作者姓名:左华  赵宝祥  王大威
作者单位:山东大学化学与化工学院有机化学研究所,山东,济南,250100
摘    要:研究了由苯甲醛、丁醛合成α 甲基肉桂醛的工艺,考察了催化剂用量、原料摩尔比、反应时间对合成α 甲基肉桂醛收率的影响。其优化条件是:以乙醇作溶剂,四丁基溴化铵为催化剂,n(苯甲醛)∶n(丙醛)∶n(催化剂)1 4∶1∶0 015,室温反应6h,收率达84 6%,且过量的苯甲醛能回收。

关 键 词:相转移催化  苯甲醛  丙醛  α-甲基肉桂醛  合成
文章编号:1009-9212(2003)06-0036-02
修稿时间:2003年6月16日

The Synthesis of α-Methylcinnamaldehyde as Intermediate of Epalrestat
ZUO Hua,etc.The Synthesis of α-Methylcinnamaldehyde as Intermediate of Epalrestat[J].Fine Chemical Intermediates,2003,33(6):36-37.
Authors:ZUO Hua  etc
Abstract:The influence factors on the yield of α-methylcinnamaldehyde, such as kind of catalysts, dosage of catalyst, molar ratio of benzaldehyde to n propylaldehyde, and reaction time were investigated. The optimum preparation conditions are as follows∶n(benzaldehyde)∶n(n propylaldehyde)∶n(catalyst)=1.4∶1∶0.015, 6 h of reaction time with ethanol as solvent, tetrabutylammonium bromide as catalyst, and reacting at room temperature. The yield of α methylcinnamaldehyde reaches 84.6%, and surplus benzaldehyde could be used recyclely.
Keywords:phase transfer catalysis  α-methylcinnamaldehyde  synthesis
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