第 33 卷第 6 期Vol. 33 No. 6
2003 年 12 月Dec 2003

所属栏目:其它

依帕司他中间体α-甲基肉桂醛的合成
左华; 赵宝祥; 王大威(山东大学化学与化工学院有机化学研究所; 山东济南)
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
中图分类号:TQ224.13  文献标识码:A  文章编号:1009-9212(2003)06-0036-02
The Synthesis of α-Methylcinnamaldehyde as Intermediate of Epalrestat
ZUO Hua; etc(Institute of Organic Chemistry; School of Chemistry and Chemical Engineering Shandong University; Jinan Shandong 250100; China)
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 b...
Key words:phase transfer catalysis; α-methylcinnamaldehyde; synthesis
收稿日期:2003-06-16
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