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使用多相催化剂通过需氧分子内氧化偶联反应合成N-取代的2,3,6,7-四甲氧基咔唑

Aerobic Intramolecular Oxidative Coupling Using Heterogeneous Catalyst for Synthesis of N-Substituted 2,3,6,7-Tetramethoxycarbazoles.

作者信息

Matsumoto Kenji, Kobayashi Yoshinori, Hirokane Tsukasa, Yoshida Masahiro

机构信息

Faculty of Pharmaceutical Sciences, Tokushima Bunri University.

出版信息

Chem Pharm Bull (Tokyo). 2020;68(2):167-172. doi: 10.1248/cpb.c19-00947.

Abstract

A heterogeneous metal catalyst enabled the intramolecular oxidative coupling of diarylamines to form carbazoles with molecular oxygen as the sole oxidant. Rh/C had efficient catalytic activity and allowed the catalyst loading to be reduced to 0.1 mol% while maintaining excellent yields of carbazoles. This reaction is operationally simple in an open-to-air setup, and provides a green and atom-economical process for an efficient synthetic approach to N-substituted carbazoles.

摘要

一种多相金属催化剂能够实现二芳基胺的分子内氧化偶联反应,以分子氧作为唯一氧化剂生成咔唑。Rh/C具有高效的催化活性,可将催化剂负载量降低至0.1 mol%,同时保持咔唑的优异产率。该反应在开放式空气中操作简单,为N-取代咔唑的高效合成提供了一种绿色且原子经济的方法。

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