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首页> 外文期刊>Catalysis Letters >Facile and Efficient Reductive Homocoupling of Benzyl and Aryl Halides Catalyzed by Ionic Liquid [C_(12)mim][CuCl2] in the Presence of Metallic Zinc and Copper
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Facile and Efficient Reductive Homocoupling of Benzyl and Aryl Halides Catalyzed by Ionic Liquid [C_(12)mim][CuCl2] in the Presence of Metallic Zinc and Copper

机译:金属锌和铜存在下离子液体[C_(12)mim] [CuCl2]催化苄基卤化物和芳基卤化物的高效还原反应

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摘要

A facile and efficient synthesis of bibenzyl and biaryl derivatives by reductive homocoupling reaction is described. Treatment of benzyl and aryl halides with metallic zinc and copper powder in the presence of a catalytic amount of [C_(12)mim][CuCl2] under ligand- and base-free conditions gives the corresponding bibenzyls and biaryls in good to high yields. The product can be isolated by a simple extraction with organic solvent, and the catalytic system can be recycled or reused without any significant loss of catalytic activity.
机译:描述了通过还原性均偶联反应容易且有效地合成联苄基和联芳基衍生物。在无配体和无碱的条件下,在催化量的[C_(12)mim] [CuCl2]存在下,用金属锌和铜粉处理苄基卤化物和芳基卤化物,可以得到高至高收率的相应联苄基和联芳基。可以通过简单地用有机溶剂萃取来分离产物,并且催化体系可以循环使用,而不会明显降低催化活性。

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