Highly Efficient and Facile Method for Synthesis of 2-Substituted Benzimidazoles via Reductive Cyclization of O-Nitroaniline and Aryl Aldehydes

H. Naeimi, Nasrin Alishahi
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引用次数: 5

Abstract

A versatile and convenient synthesis of 2-substituted benzimidazoles, using o-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.
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邻硝基苯胺和芳基醛还原环化合成2-取代苯并咪唑的高效简便方法
以邻硝基苯胺为原料,以几种芳基醛为原料,用少量不情愿剂合成了2-取代苯并咪唑。该反应是在非常温和的室温条件下进行的。在相当短的反应时间内获得了很好的产率。
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