Improving palladium-catalyzed cyanation of aryl halides: development of a state-of-the-art methodology using potassium hexacyanoferrate(II) as cyanating agent

被引:188
作者
Schareina, T [1 ]
Zapf, A [1 ]
Beller, M [1 ]
机构
[1] Univ Rostock eV, Leibniz Inst Organ Katalyse, D-18055 Rostock, Germany
关键词
aryl halides; benzonitriles; cyanation; homogeneous catalysis; palladium; potassium hexacyanoferrate(II);
D O I
10.1016/j.jorganchem.2004.08.020
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Benzonitriles are easily accessible via palladium-catalyzed cyanation of aryl halides using potassium hexacyanoferrate(II) as cyanide source. This method is applicable on both activated and deactivated aryl and heteroaryl bromides and activated chlorides giving the corresponding benzonitriles in good to excellent yield. Advantageously, the used cyanating agent is non-toxic and cheap. The presented catalyst system is rather simple and it is not necessary to add expensive phosphines, making the novel method also attractive for industrial applications. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:4576 / 4583
页数:8
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