摘要
以取代苯甲酸和苯甲酰肼为原料,丙基磷酸环酐为缩合剂和脱水剂,三乙胺为碱性介质,研究了环缩合反应一步法制备6种1,3,4-噁二唑化合物的合成工艺,其结构经IR和1HNMR以及元素分析测试技术加以确证,合成收率为88%~94%。
A general,mild and efficient method to synthesize six1,3,4-oxadiazoles(3a-f) in one-pot procedure by condensation between the carboxylic acids and the respective hydrazides at triethylamine alkaline solution in the presence of propylphosphonic anhydride was discussed.The structure of products was confirmed by IR,1HNMR and elemental analysis,yielding in within 88%~94% respectively.
出处
《化学试剂》
CAS
CSCD
北大核心
2011年第10期942-944,共3页
Chemical Reagents
基金
天津市高等学校科技发展基金资助项目(2008-0509)
关键词
苯甲酸
苯甲酰肼
1
3
4-噁二唑
丙基磷酸环酐
benzoic acid
benzoyl hydrazine
1
3
4-oxadiazoles
propylphosphonic anhydride