Development of new palladium catalysts for the alkoxycarbonylation of aryl chlorides

被引：84

作者：

Mägerlein, W

Indolese, AF

Beller, M

机构：

[1] Univ Rostock EV, Inst Organ Katalyseforschung IfOK, D-18055 Rostock, Germany

[2] Solvias AG, CH-4002 Basel, Switzerland

来源：

JOURNAL OF ORGANOMETALLIC CHEMISTRY | 2002年 / 641卷 / 1-2期

关键词：

carbonylation; palladium; ferrocenyl phosphines; aryl chlorides; homogeneous catalysis; benzoic acids;

D O I：

10.1016/S0022-328X(01)01293-1

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

The alkoxycarbonylation of different aryl chlorides was studied. Studies of the butoxycarbonylation of 4-chlorobenzotrifluoride and chlorobenzene using chelating ferrocenylphosphines reveal the advantages of these ligands compared to the wen-known tricyclohexylphosphine (PCy3). (1-(2-(Dicyclohexylphosphino)ferroceuyl)ethyldicyclohexylphosphine (4) was shown to give the most active palladium catalyst system. The usefulness of this catalyst is demonstrated in the alkoxycarbonylation of various aryl chlorides. Optimized carbonylation conditions were realized by a statistical design of three critical reaction parameters. (C) 2002 Elsevier Science B.V. All rights reserved.

引用

页码：30 / 40

页数：11

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