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首页> 外文期刊>RSC Advances >One pot synthesis of 1,2,4,5-tetrasubstituted-imidazoles catalyzed by trityl chloride in neutral media
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One pot synthesis of 1,2,4,5-tetrasubstituted-imidazoles catalyzed by trityl chloride in neutral media

机译:三苯甲基氯在中性介质中一锅合成1,2,4,5-四取代-咪唑

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摘要

Trityl chloride (TrCl or Ph3CCl) efficiently catalyzes the one-pot multi-component condensation of benzil with aldehydes, primary amines and ammonium acetate under neutral and solvent-free conditions to give 1,2,4,5-tetrasubstituted imidazoles in high to excellent yields and in short reaction times. Mechanistically, it is attractive that trityl chloride promotes the reaction by in situ generation of trityl carbocation (Ph3C+).
机译:三苯甲基氯(TrCl或Ph3CCl)可在中性和无溶剂条件下有效催化苯甲酰与醛,伯胺和乙酸铵的一锅多组分缩合反应,得到高,极好的1,2,4,5-四取代的咪唑收率高,反应时间短。从机理上讲,三苯甲基氯通过原位生成三苯甲基碳正离子(Ph3C +)促进反应。

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