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采用可重复使用的铁催化剂选择性还原硝基芳烃,从硝基芳烃和羰基化合物直接合成亚胺、苯并咪唑和喹喔啉。

The Direct Synthesis of Imines, Benzimidazoles and Quinoxalines from Nitroarenes and Carbonyl Compounds by Selective Nitroarene Hydrogenation Employing a Reusable Iron Catalyst.

机构信息

Anorganische Chemie II-Katalysatordesign, Universität Bayreuth, 95440, Bayreuth, Germany.

出版信息

Chemistry. 2018 Jun 26;24(36):8989-8993. doi: 10.1002/chem.201801525. Epub 2018 May 25.

DOI:10.1002/chem.201801525
PMID:29668069
Abstract

The "replacement" of noble metals by earth abundant metals is a desirable aim in catalysis and a possible way of conserving rare elements. The "replacement" is especially attractive if novel selectivity patterns are observed permitting the development of novel coupling reactions. Herein, we report on a novel, robust and reusable iron catalyst, which permits the selective hydrogenation of nitroarenes in the presence of hydrogenation-sensitive functional groups. Based on the selectivity pattern observed, the direct iron-catalyzed synthesis of imines and benzimidazoles from nitroarenes and aldehydes becomes feasible. In addition, we introduce the direct synthesis of quinoxalines from nitroarenes and diketones applying our catalyst.

摘要

用丰富的地球金属取代贵金属是催化中一个理想的目标,也是一种保存稀有元素的可行方法。如果观察到新的选择性模式,允许开发新的偶联反应,这种“取代”就特别有吸引力。在此,我们报告了一种新型的、稳健的和可重复使用的铁催化剂,它可以在存在加氢敏感官能团的情况下选择性地氢化硝基芳烃。根据观察到的选择性模式,从硝基芳烃和醛直接铁催化合成亚胺和苯并咪唑成为可能。此外,我们还介绍了应用我们的催化剂从硝基芳烃和二酮直接合成喹喔啉。

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