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近临界水中苯甲醛与丙酮的Claisen-Schmidt缩合反应
引用本文:朱志强,曾健青,刘莉玫. 近临界水中苯甲醛与丙酮的Claisen-Schmidt缩合反应[J]. 广州化学, 2002, 27(2): 17-20
作者姓名:朱志强  曾健青  刘莉玫
作者单位:中国科学院广州化学研究所,广东,广州,510650
基金项目:广东省自然科学基金资助项目(990749)
摘    要:在近临界水中进行有机合成为可持续化学合成提供了新的途径。对近临界水中苯甲醛与丙酮的Claisen-Schmidt缩合反应的研究表明,在没有外加任何催化剂的条件下,苯甲醛与丙酮可顺利地发生缩合反应,近临界水在其中兼作溶剂和催化剂,避免了碱催化剂的使用和随后繁杂的中和、分离步骤以及产生废弃盐等弊端。温度、反应时间和初始水量对反应的转化率和苯丁烯酮的产率有不同的影响。

关 键 词:近临界水  苯甲醛  丙酮  Claisen-Schmidt缩合反应
文章编号:1009-220(2002)02-0017-04
修稿时间:2001-10-23

Claisen-Schmidt Condensation Reaction of Benzaldehyde and Acetone in Near-critical Water
ZHU Zhi-qiang,ZENG Jian-qing,LIU Li-mei. Claisen-Schmidt Condensation Reaction of Benzaldehyde and Acetone in Near-critical Water[J]. Guangzhou Chemistry, 2002, 27(2): 17-20
Authors:ZHU Zhi-qiang  ZENG Jian-qing  LIU Li-mei
Affiliation:ZHU Zhi-qiang,ZENG Jian-qing*,LIU Li-mei
Abstract:To perform organic synthesis in near-critical water offers a new opportunity for the development of sustainable chemical synthetic process. Investigation of Claisen-Schmidt condensation reaction using near-critical water as media indicated that the reaction can be carried out in near-critical water without any added catalyst. Since near-critical water acts as both solvent and catalyst, the subsequent need for neutralization and salt disposal in the classical method were avoided. The conversion of benzaldehyde and yield of benzylidene acetone were influenced by reaction time, temperature and initial water volume.
Keywords:near-critical water  benzaldehyde  acetone  Claisen-Schmidt condensation reaction  
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