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使用 N-亚硝糖精轻松获得硝基芳烃和硝基杂芳烃。

Facile access to nitroarenes and nitroheteroarenes using N-nitrosaccharin.

机构信息

Department of Chemistry and Applied Biosciences, ETH Zürich, Vladimir-Prelog-Weg 2, 8093, Zürich, Switzerland.

出版信息

Nat Commun. 2019 Jul 30;10(1):3410. doi: 10.1038/s41467-019-11419-y.

Abstract

Nitroaromatics and nitroheteroaromatics serve as key building blocks and intermediates in synthesis, and form the core scaffold of a vast number of materials, dyes, explosives, agrochemicals and pharmaceuticals. However, their synthesis relies on harsh methodologies involving excess mineral acids, which present a number of critical drawbacks in terms of functional group compatibility and environmental impact. Modern, alternative strategies still suffer from significant limitations in terms of practicality, and a general protocol amenable to the direct C-H functionalization of a broad range of aromatics has remained elusive. Herein we introduce a bench-stable, inexpensive, easy to synthesize and recyclable nitrating reagent based on saccharin. This reagent acts as a controllable source of the nitronium ion, allowing mild and practical nitration of both arenes and heteroarenes displaying an exceptional functional group tolerance.

摘要

硝芳烃和硝杂芳烃可用作合成的关键构建模块和中间体,并形成大量材料、染料、炸药、农用化学品和药物的核心支架。然而,它们的合成依赖于苛刻的方法,涉及过量的矿物酸,这在官能团兼容性和环境影响方面存在许多关键的缺点。现代的替代策略在实用性方面仍然存在显著的局限性,并且一种能够直接实现广泛芳香族化合物 C-H 功能化的通用方案仍然难以实现。在此,我们介绍了一种基于甜蜜素的稳定、廉价、易于合成和可回收的硝化试剂。该试剂可作为硝鎓离子的可控源,允许对具有出色官能团耐受性的芳烃和杂芳烃进行温和且实用的硝化反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3685/6667458/3f92f282eb2d/41467_2019_11419_Fig1_HTML.jpg

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