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在温和条件下,水相中高效可回收的 CuI 纳米粒子催化的硫醇与芳基卤化物的 S-芳基化反应。

Efficient recyclable CuI-nanoparticle-catalyzed S-arylation of thiols with aryl halides on water under mild conditions.

机构信息

School of Medical Engineering, Hefei University of Technology, Hefei 230009, P. R. China.

出版信息

Org Biomol Chem. 2012 Apr 7;10(13):2562-8. doi: 10.1039/c2ob06795a. Epub 2012 Feb 21.

Abstract

CuI nanoparticles efficiently catalyzed the C-S cross coupling of aryl and alkyl thiols with aryl halides in the absence of ligands on water under mild conditions. A wide range of diaryl sulfides and aryl alkyl sulfides are synthesized in good to excellent yields utilizing this protocol. This procedure is particularly noteworthy given its mild conditions, avoiding the undesired formation of disulfides through oxidation of thiols. The recovery and successful reutilization of the catalyst is described. Furthermore, the directed synthesis of bisarylated product is presented.

摘要

CuI 纳米粒子在温和条件下、无需配体的情况下,能有效地催化水相中芳基和烷基硫醇与芳基卤化物的 C-S 交叉偶联反应。利用该反应条件,能以良好到优异的收率合成多种二芳基硫醚和芳基烷基硫醚。鉴于该反应条件温和,避免了硫醇氧化生成二硫化物,因此该方法具有重要意义。此外,还描述了催化剂的回收和再利用。进一步地,还提出了导向合成双芳基化产物的方法。

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