研究论文

纳米钯催化的高效Suzuki偶联反应

  • 赵晓霞 ,
  • 常宏宏 ,
  • 李兴 ,
  • 魏文珑
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  • a 太原科技大学化学与生物工程学院 太原 030021;
    b 太原理工大学化学化工学院 太原 030024

收稿日期: 2015-02-14

  修回日期: 2015-06-04

  网络出版日期: 2015-06-12

基金资助

山西省自然科学基金(No. 2012021007-2)资助项目.

Nanoparticles Pd-Catalyzed Highly Efficient Suzuki Cross-Coupling Reaction

  • Zhao Xiaoxia ,
  • Chang Honghong ,
  • Li Xing ,
  • Wei Wenlong
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  • a College of Chemistry and Biological Engineering, Taiyuan University of Science and Technology, Taiyuan 030021;
    b College of Chemistry and Chemical Engineering, Taiyuan University of Technology, Taiyuan 030024

Received date: 2015-02-14

  Revised date: 2015-06-04

  Online published: 2015-06-12

Supported by

Project supported by the Natural Science Foundation of Shanxi Province (No. 2012021007-2).

摘要

开发了一种使用Al2O3作载体, 由四三苯基膦钯制备的纳米钯催化剂催化的高效绿色Suzuki 反应来合成联苯类化合物的方法. 该反应体系以DMF和H2O的混合体系作反应溶剂, 在空气中于25~90 ℃下, 催化剂可高效催化卤代芳烃与芳基硼酸的Suzuki偶联反应, 所有考察的反应底物都给出很高的收率, 并且催化剂循环利用6次后, 其催化活性和反应收率都没有明显降低.

本文引用格式

赵晓霞 , 常宏宏 , 李兴 , 魏文珑 . 纳米钯催化的高效Suzuki偶联反应[J]. 有机化学, 2015 , 35(8) : 1650 -1656 . DOI: 10.6023/cjoc201502022

Abstract

An efficient protocol for the Suzuki reactions catalyzed by Pd(PPh3)4-derived nanoparticles palladium catalyst has been developed. This method is able to prepare a variety of biaryls under air atmosphere at 25~90 ℃ in DMF/H2O mixture solvent. In the presence of this catalyst, the cross-coupling reactions of aryl halides with arylboronic acids proceed smoothly and afforded the desired coupling products with high yields. The catalyst could be recycled 6 times without loss of activity and decrease of yield.

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