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苄醇的光催化直接对位选择性C-H胺化反应:选择性与侧链取代基无关。

Photocatalytic Direct Para-Selective C-H Amination of Benzyl Alcohols: Selectivity Independent of Side Substituents.

作者信息

Liu Donghan, Tu Ting, Zhang Tinglei, Nie Guihua, Liao Tianhui, Ren Shi-Chao, Zhang Xinglong, Chi Yonggui Robin

机构信息

State Key Laboratory of Green Pesticide, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Center for R&D of Fine Chemicals of Guizhou University, Guiyang, 550025, China.

Institute of High Performance Computing, A*STAR (Agency for Science, Technology and Research), Singapore, 138632, Singapore.

出版信息

Angew Chem Int Ed Engl. 2024 Oct 21;63(43):e202407293. doi: 10.1002/anie.202407293. Epub 2024 Sep 17.

Abstract

Aminoarenes are important molecules for broad applications in nearly all modern industries that involve chemicals. Direct and site-selective C-H bond amination of arenes provides the most efficient and convenient method to prepare aminoarenes. A main challenge is to selectively install the amino group (or other functional groups) to the distal para-carbon of arenes (especially multi-substituted arenes) during the C-H bond functionalization events. Herein, we address this problem by designing a new strategy via a sequential radical dearomatization/radical amination/rearomatization process for para-selective amination of benzyl alcohols. The para-selectivity of our reaction is completely independent of the electronic and steric properties of the other substituents of the arene substrates. Aminoarenes with many substituents (up to full substitution) and diverse substitution patterns, including those difficult to synthesize previously, could be readily prepared using our protocols. Further exploration of the current strategy shall lead to other challenging C-H functionalization of arenes.

摘要

氨基芳烃是几乎所有涉及化学品的现代工业中广泛应用的重要分子。芳烃的直接和位点选择性C-H键胺化提供了制备氨基芳烃最有效和便捷的方法。一个主要挑战是在C-H键官能化过程中,将氨基(或其他官能团)选择性地安装到芳烃(特别是多取代芳烃)的远端对位碳上。在此,我们通过设计一种新策略来解决这个问题,该策略通过苄醇的顺序自由基去芳构化/自由基胺化/再芳构化过程进行对位选择性胺化。我们反应的对位选择性完全独立于芳烃底物其他取代基的电子和空间性质。使用我们的方法可以很容易地制备具有许多取代基(高达完全取代)和不同取代模式的氨基芳烃,包括那些以前难以合成的。对当前策略的进一步探索将导致芳烃其他具有挑战性的C-H官能化反应。

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