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首页> 外文期刊>Organic Chemistry International >Highly Efficient and Facile Method for Synthesis of 2-Substituted Benzimidazoles via Reductive Cyclization ofO-Nitroaniline and Aryl Aldehydes
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Highly Efficient and Facile Method for Synthesis of 2-Substituted Benzimidazoles via Reductive Cyclization ofO-Nitroaniline and Aryl Aldehydes

机译:邻硝基苯胺和芳醛的还原环化合成2-取代的苯并咪唑的高效简便方法

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摘要

A versatile and convenient synthesis of 2-substituted benzimidazoles, usingo-nitroaniline as starting material with several aryl aldehydes, has been accomplished by using a small amount of a reluctant agent. The reaction was carried out under very mild conditions at room temperature. The yields obtained are very good in reasonably short reaction times.
机译:使用邻硝基苯胺作为起始原料与几种芳基醛的通用合成2-取代苯并咪唑的方法是,通过使用少量的抗性剂来完成。该反应在非常温和的条件下在室温下进行。在相当短的反应时间内,获得的收率非常好。

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