Issue 16, 2025

Polynaphthoquinone mediated metal-free direct N-alkylation of (hetero)aryl amines using alcohols

Abstract

Herein, we present polynaphthoquinone as an effective metal-free catalyst for the direct N-alkylation of aryl and heteroaryl amines using alcohols. Our experiments reveal that the optimal reaction conditions consist of 1.0 mmol of alcohol, 1.5 mmol of aniline, 0.8 equivalents of t-BuOK, and 30 wt% polynaphthoquinone catalyst in toluene at 135 °C under an inert atmosphere for 24 hours. Control experiments confirm that without a catalyst or base, the reaction fails to progress. Additionally, the reused catalyst in subsequent reactions yields good to excellent results. This methodology has also been extended to the dehydrogenative synthesis of quinolines and indoles.

Graphical abstract: Polynaphthoquinone mediated metal-free direct N-alkylation of (hetero)aryl amines using alcohols

Supplementary files

Article information

Article type
Paper
Submitted
28 Jan 2025
Accepted
14 Mar 2025
First published
19 Mar 2025

Org. Biomol. Chem., 2025,23, 3875-3880

Polynaphthoquinone mediated metal-free direct N-alkylation of (hetero)aryl amines using alcohols

U. K. Panigrahi and V. K. M. Ramakrishnan, Org. Biomol. Chem., 2025, 23, 3875 DOI: 10.1039/D5OB00163C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements