摘要
在水介质中,醛或酮首先和邻氨基苯甲酰肼反应形成腙;在1 mol%Yb(OTf)3催化下,再与另外一分子醛或酮反应,构建一系列不同取代的喹唑啉酮衍生物.该方法具有中性反应条件、产率高(80%~94%)、操作简单和环境友好等优点.产物的结构通过IR,1H NMR和HRMS表征.
Using water as a green reaction media,aldehydes or ketones react with 2-aminobenzohydrazide to give hydrazone firstly,and then a series of quinazolinone derivatives are obtained by the reaction of the hydrazone with another molecule of aldehyde or ketone catalyzed by 1 mol% Yb(OTf)3.This method provides several advantages such as neutral conditions,high yields(80%~94%),simple work-up and environmental benignity.The structures were established by spectroscopic data of IR,1H NMR and HRMS techniques.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2011年第9期1522-1526,共5页
Chinese Journal of Organic Chemistry
基金
江苏省高校自然科学基金(No.08KJD150019)
江苏省"青蓝工程"创新团队(No.08QLT001)资助项目