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β-酮酸酯类化合物与丁烯酮的Micheal加成反应研究
引用本文:李晨辉,鲍莹,张辉,刘建宇,许永男.β-酮酸酯类化合物与丁烯酮的Micheal加成反应研究[J].辽宁化工,2014(10):1236-1237.
作者姓名:李晨辉  鲍莹  张辉  刘建宇  许永男
作者单位:沈阳药科大学教育部基于靶点的药物设计与研究重点实验室;
摘    要:2-氧代环戊烷甲酸甲酯或2-氧代环己烷甲酸甲酯与短链α,β-不饱和羰基化合物丁烯酮在六水合三氯化铁催化、无溶剂条件下进行Michael加成反应,能有效避免副反应的发生。该方法也可应用于其他β-酮酸酯类化合物,反应简便易行,收率高。所得到化合物结构均经1H-NMR和MS谱确证。

关 键 词:β-酮酸酯  Micheal加成反应  α  β-不饱和酮

Michael Addition Reaction of β-Keto Esters and Methyl Vinyl Ketone
Affiliation:LI Chen-hui;BAO Ying;ZHANG Hui;LIU Jian-yu;XV Yong-nan;Key Laboratory of Structure-Based Drug Design and Discovery, Ministry of Education, Shenyang Pharmaceutical University;
Abstract:Using ferric chloride hexahydrate as the catalyst, the Michael addition reaction between esters of 2-oxocyclopentanecarboxylic acid and short chain α,β-unsaturated carbonyl compound under solvent free conditions was carried out, the side reactions were effectively avoided. And the product was characterized by 1H-NMR and mass spectrometry. The method has simple operation and high yield.
Keywords:β-keto esters  Michael addition reaction  short chain α  β-unsaturated carbonyl compounds
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