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Improved Preparation of Tyramine by Curtius Rearrangement
An improved and facile preparation of tyramine [2-(p-hydroxyphenyl)ethylamine] was described, which starts from phenol and acrylonitrile to form β-(p-hydroxyphenyl) propionic acid via Friedel-Craft's alkylation and nitrile hydrolysis. After hydrazinolysis and a subsequent Curtius rearrangement, tyramine was obtained in 30.2% total yield.
作 者: LI Yun YANG Fan XU Xiaoying PAN Shiyin WANG Lixin XIA Chuanqin 作者单位: LI Yun,YANG Fan,XIA Chuanqin(Department of Chemistry,Sichuan University,Chengdu,Sichuan 610041,China)XU Xiaoying,PAN Shiyin,WANG Lixin(Key Laboratory of Asymmetric Synthesis & Chirotechnology of Sichuan Province and National Engineering Research Center of Chiral Drugs,Chengdu Institute of Organic Chemistry,Chinese Academy of Sciences,Chengdu,Sichuan 610041,China)
刊 名: 中国化学(英文版) SCI 英文刊名: CHINESE JOURNAL OF CHEMISTRY 年,卷(期): 2009 27(2) 分类号: O6 关键词: preparation tyramine β-(p-hydroxyphenyl)propionic acid curtius rearrangement【Improved Preparation of Tyramine by 】相关文章:
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