An efficient and recyclable iron(III)-containing imidazolium salt catalyst for cross-coupling of aryl Grignard reagents with alkyl halides |
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Authors: | ChunHui Yan LinLin Wang HuanHuan Gao HongMei Sun Qi Shen |
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Institution: | 1. The Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou, 215123, China
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Abstract: | 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride, DIPrim]Cl, was used to produce a novel iron(III)-containing imidazolium salt DIPrim]FeCl 4 ], which included a N,N-diarylimidazolium cation (R = 2,6-diisopropylphenyl), DIPrim] + , and tetrachloroferrate(III) anion, FeCl 4 ]. This compound was an effective and easy-to-use catalyst for the cross-coupling of aryl Grignard reagents with primary and secondary alkyl halides bearing -hydrogens. After simply decanting the cross-coupling product in the ether layer, DIPrim]FeCl 4 ] could be reused in at least four successive runs without significant loss of catalytic activity. |
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Keywords: | iron(III) complex imidazolium salt alkyl halide cross-coupling Grignard reagent |
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