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Iron-catalyzed protodehalogenation of alkyl and aryl halides using hydrosilanes

机译:使用氢化硅烷铁催化烷基卤化物和芳基卤化物的原脱卤

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摘要

A simple and efficient iron-catalyzed protodehalogenation of alkyl and aryl halides using phenylhydrosilane is disclosed. The reaction utilizes FeCl3 without the requirement of ligands. Unactivated alkyl and aryl halides were successfully reduced in good yields; sterically hindered tertiary halides were also reduced including the less reactive chlorides. The scalability of this methodology was demonstrated by a gram-scale synthesis with a catalyst loading as low as 0.5 mol%. Notably, disproportionation of phenylsilane leads to diphenylsilane that further reduces the halides. Preliminary mechanistic studies revealed a non-radical pathway and the source of hydrogen is PhSiH3 via deuterium labeling studies. Our methodology represents simplicity and provides a good alternative to typical tin, aluminum and boron hydride reagents.
机译:公开了使用苯基氢硅烷的烷基铁和芳基卤的简单有效的铁催化的原脱卤。该反应利用FeCl 3而不需要配体。未活化的烷基卤和芳基卤化物以良好的收率成功还原。位阻叔卤化物也被还原,包括反应性较低的氯化物。这种方法的可扩展性通过克级合成证明,催化剂的负载量低至0.5摩尔%。明显地,苯基硅烷的歧化导致二苯基硅烷,其进一步减少了卤化物。初步的机理研究表明,通过氘标记研究表明氢是PhSiH3,这是非自由基途径。我们的方法简单明了,是典型的氢化锡,氢化铝和氢化硼试剂的良好替代品。

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  • 来源
    《Organic & biomolecular chemistry》 |2019年第7期|1749-1753|共5页
  • 作者单位

    Indian Inst Sci Educ & Res, Sch Chem, Thiruvananthapuram 695551, Kerala, India;

    Indian Inst Sci Educ & Res, Sch Chem, Thiruvananthapuram 695551, Kerala, India;

    Indian Inst Sci Educ & Res, Sch Chem, Thiruvananthapuram 695551, Kerala, India;

    Indian Inst Sci Educ & Res, Sch Chem, Thiruvananthapuram 695551, Kerala, India;

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