Microwave-Assisted Amination from Aryl Triflates without Base and Catalyst

Gang Xu and Yan-Guang Wang*
Department of Chemistry, Zhejiang University, Hangzhou 310027, P. R. China
Org. Lett., 2004, 6 (6), pp 985–987
DOI: 10.1021/ol049963j
Publication Date (Web): February 21, 2004
Copyright © 2004 American Chemical Society

Abstract

Abstract Image

Aryl triflates are effectively converted to the corresponding anilines under microwave irradiation in 1-methyl-2-pyridone (NMP) without base and catalyst. Aryl triflates substituted with both electron-poor and electron-rich groups give good to excellent yields. It is noteworthy that the halogenated aryl triflates can chemoselectively react with amines to afford halogenated anilines.

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History

  • Published In Issue March 18, 2004
  • Received January 6, 2004

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