A metal-free porous organic polymer-based heterogeneous catalyst for the borrowing hydrogen-mediated N-alkylation of sulfonamides with alcohols

Abstract

The development of green and sustainable borrowing hydrogen catalysis without using expensive and toxic metals is a challenging task. Herein, a highly stable, low-cost, metal-free heterogeneous carbocatalyst has been developed for the first time to mediate the N-alkylation of sulfonamides with alcohols via borrowing hydrogen catalysis. The designed 1,10-phenanthroline (Phen)-functionalized porous organic polymer-based carbocatalyst (Phen-POP) efficiently produces N-alkylated sulfonamides in good yields, performing on par with the transition-metal-based catalysts. Computational studies show that the electronegative N present in the Phen unit pulls the electron density from the adjacent C atom, making it more electron-deficient, which in turn boosts the transfer of hydride to the substrates. The prepared Phen-POP catalyst is highly robust and can be reused for at least five cycles without significant activity loss. Further, a scalable protocol has been successfully demonstrated at the gram-scale (5.0 g) with isolation of pure product without any chromatography. Therefore, this work provides a promising module to realize the synthesis of N-alkylated sulfonamides with alcohols on an industrial scale, and a design strategy to develop metal-free systems for many other borrowing hydrogen catalysis.

Graphical abstract: A metal-free porous organic polymer-based heterogeneous catalyst for the borrowing hydrogen-mediated N-alkylation of sulfonamides with alcohols

Supplementary files

Article information

Article type
Paper
Submitted
10 May 2025
Accepted
30 Jun 2025
First published
01 Jul 2025

Catal. Sci. Technol., 2025, Advance Article

A metal-free porous organic polymer-based heterogeneous catalyst for the borrowing hydrogen-mediated N-alkylation of sulfonamides with alcohols

R. Vijay, D. Yogesh, R. Shanmugam, N. Lingaiah, T. Ponpandian and G. H. Gunasekar, Catal. Sci. Technol., 2025, Advance Article , DOI: 10.1039/D5CY00562K

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