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铜-偕二膦催化未活化烷烃通过C(sp)-H活化的直接酰胺化反应

Cu-Amidobis(phosphine)-Catalyzed Direct Amidation of Unactivated Alkanes via C(sp)-H Activation.

作者信息

Sonawane Sachin C, Sabharwal Gazal, Balakrishna Maravanji S

机构信息

Phosphorus Laboratory, Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai 400076, India.

出版信息

Org Lett. 2024 Jun 7;26(22):4589-4593. doi: 10.1021/acs.orglett.4c01063. Epub 2024 May 28.

Abstract

Herein, we describe an acid-base-free, sustainable, and efficient method for direct amidation of unactivated alkanes and toluene derivatives, using the dimeric Cu complex [Cu{-PhPCHCONCHPPh-}] (here onward referred to as [PNP-Cu]). Using this method, C(sp)-N bond formation was achieved through the activation of very challenging C(sp)-H bonds in cycloalkanes, alkenes, allyl groups, and benzyl groups, with tolerance toward ketonic groups, heterocycles, and halide functionalities. One of the precatalysts, (PNHP-Cu-Npht) was isolated and structurally characterized. Isomerization in allyl-functionalized alkanes and selective benzylic alkylation in ketones were observed. This is a novel method for C(sp)-N bond formation via direct N-alkylation of phthalimide, sulfonamide, benzamide, and phosphamidate.

摘要

在此,我们描述了一种无酸碱、可持续且高效的方法,用于未活化烷烃和甲苯衍生物的直接酰胺化反应,该方法使用二聚铜配合物[Cu{-PhPCHCONCHPPh-}](以下简称[PNP-Cu])。通过该方法,通过活化环烷烃、烯烃、烯丙基和苄基中极具挑战性的C(sp)-H键实现了C(sp)-N键的形成,该方法对酮基、杂环和卤化物官能团具有耐受性。其中一种预催化剂(PNHP-Cu-Npht)被分离并进行了结构表征。观察到烯丙基官能化烷烃中的异构化以及酮中的选择性苄基烷基化。这是一种通过邻苯二甲酰亚胺、磺酰胺、苯甲酰胺和磷酸酰胺的直接N-烷基化形成C(sp)-N键的新方法。

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