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首页> 外文期刊>European journal of organic chemistry >Synthesis of Symmetrical Diaryl Ketones by Cobalt-Catalyzed Reaction of Arylzinc Reagents with Ethyl Chloroformate
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Synthesis of Symmetrical Diaryl Ketones by Cobalt-Catalyzed Reaction of Arylzinc Reagents with Ethyl Chloroformate

机译:钴锌试剂与氯甲酸乙酯的钴催化反应合成对称的二芳基酮

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摘要

Symmetrical diaryl ketones were prepared by a cross-coupling reaction between aryl bromides and ethyl chloroformate. This new method, which uses a catalyst composed of CoBr2 and a bipyridine ligand along with readily available starting materials, allows for the synthesis of a variety of symmetrical diaryl ketones in moderate to excellent yields (37-99%) under mild conditions. This reaction, in which ethyl chloroformate acts as a surrogate of carbon monoxide in the presence of cobalt and zinc, represents an interesting alternative to previously known approaches for the synthesis of diarylmethanones.
机译:通过芳基溴化物和氯甲酸乙酯之间的交叉偶联反应制备对称的二芳基酮。这种新方法使用由CoBr2和联吡啶配体组成的催化剂,以及容易获得的起始原料,可以在温和条件下以中等至极好的收率(37-99%)合成多种对称的二芳基酮。在钴和锌的存在下,氯甲酸乙酯充当一氧化碳的替代物的该反应代表了先前已知的合成二芳基甲烷的方法的有趣替代。

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