首页 | 本学科首页   官方微博 | 高级检索  
     

缺电子芳香三氟甲磺酸酯与胺的氯化锌配合物的交叉偶联反应
引用本文:徐娟,史大昕,魏真,魏莹菲,张奇,李加荣. 缺电子芳香三氟甲磺酸酯与胺的氯化锌配合物的交叉偶联反应[J]. 有机化学, 2012, 0(4): 776-780
作者姓名:徐娟  史大昕  魏真  魏莹菲  张奇  李加荣
作者单位:北京理工大学化工与环境学院 北京100081
摘    要:采用新型的有机胺氯化锌配合物作为缺电子芳香三氟甲磺酸酯转化成芳胺的试剂,研究发现反应可以在二甲基亚砜和碳酸钾的作用下进行,无需隔氧、密封,也不必加入配体.提出了不同于经典SNAr过程的机理,并对生成的胺化产物进行了IR,MS和1H NMR表征.

关 键 词:芳香C—N键的构建  芳胺  缺电子芳香三氟甲磺酸酯  胺的氯化锌配合物

Ligand-Free Cross-Coupling of Electron-Poor Aryl Triflates with ZnCl2 Complexes of Amines
Xu, Juan , Shi, Daxin , Wei, Zhen , Wei, Yingfei , Zhang, Qi , Li, Jiarong. Ligand-Free Cross-Coupling of Electron-Poor Aryl Triflates with ZnCl2 Complexes of Amines[J]. Chinese Journal of Organic Chemistry, 2012, 0(4): 776-780
Authors:Xu   Juan    Shi   Daxin    Wei   Zhen    Wei   Yingfei    Zhang   Qi    Li   Jiarong
Affiliation:Xu,Juan Shi,Daxin Wei,Zhen Wei,Yingfei Zhang,Qi Li,Jiarong(School of Chemical Engineering and Environment,Beijing Institute of Technology,Beijing 100081)
Abstract:The efficient conversion of electron-poor aryl triflates to the corresponding aromatic amines was accomplished by using ZnCl2 complexes of organic amines as nitrogen source with K2CO3 as the base in DMSO.The coupling reaction was performed in air and ligand-free without the sealed vessel.A possible mechanism,which was different with aromatic nucleophilic substitution(SNAr),was proposed.The amination products were confirmed by1H NMR,IR and MS techniques.
Keywords:formation of aromatic C—N bond  aromatic amine  electron-poor aryl triflates  ZnCl2complexes of amines
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号