Uncatalyst and Solvent-Free Knoevenagel Condensation Reaction at Room Temperature
Knoevenagel冷凝
化学
有机化学
催化作用
作者
心伟 何
出处
期刊:Journal of Organic Chemistry Research [Hans Publishers] 日期:2013-01-01卷期号:01 (03): 9-12
标识
DOI:10.12677/jocr.2013.13003
摘要
本文报道了芳香醛和丙二腈在室温无催化剂无溶剂下的Knoevenagel缩合反应,合成了系列苄叉基化合物,产率良好,并利用1HNMR和13CNMR等对合成的化合物结构进行了表征。结果表明,该方法没有使用催化剂和有毒有害的有机溶剂,具有反应条件温和,实验操作及产物后处理简单,产率高,对环境无污染等优点。
This paper reported the solvent-free Knoevenagel condensation of aromatic aldehydes and malononitrile at room temperature without catalyst, a series of benzylidene compounds were synthesized in high yields. Structure of all compounds was analyzed by 1HNMR, 13CNMR, and IR. The results showed that this method has advantages of mild reaction conditions and that the operation is simple, convenient post-processing, high yield, and friendly to environment.