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

机译:改善钯催化的芳基卤化物的氰化作用:使用六氰合铁酸钾(II)作为氰化剂的最新方法的开发

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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.
机译:使用六氰合铁酸钾(II)作为氰化物源,可通过钯催化的芳基卤化物的氰化反应轻松获得苯甲腈。该方法适用于活化和失活的芳基和杂芳基溴化物以及活化的氯化物,从而以良好或优异的收率得到相应的苄腈。有利地,所使用的氰化剂是无毒且便宜的。所提出的催化剂体系相当简单,并且不必添加昂贵的膦,使得该新方法也对工业应用具有吸引力。 (C)2004 Elsevier B.V.保留所有权利。

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