Phosphine-Free Palladium Acetate Catalyzed Suzuki Reaction in Water

Leifang Liu, Yuhong Zhang,* and Yanguang Wang
Department of Chemistry, Zhejiang University, Hangzhou 310027, P.R. China yhzhang@zjuem.zju.edu.cn
J. Org. Chem., 2005, 70 (15), pp 6122–6125
DOI: 10.1021/jo050724z
Publication Date (Web): June 29, 2005
Copyright © 2005 American Chemical Society

Abstract

Abstract Image

Pd(OAc)2 in a mixture of water and poly(ethylene glycol) (PEG) is shown to be an extremely active catalyst for the Suzuki reaction of aryl iodides and bromides. The reaction can be conducted under mild conditions (50 °C) without the use of a microwave or phosphine ligand in high yields. The isolation of the products is readily performed by the extraction of diethyl ether, and the Pd(OAc)2−PEG can be reused without significant loss in activity.

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History

  • Published In Issue July 22, 2005
  • Received April 12, 2005

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