Issue 9, 2022

An expedient, efficient and solvent-free synthesis of T3P®-mediated amidation of benzhydrols with poorly reactive N-nucleophiles under MW irradiation

Abstract

An expedient, efficient, economical, environmentally benign, and solvent free amidation protocol of benzhydrols with less reactive nitrogen nucleophiles assisted by propylphosphonic anhydride (T3P®) under microwave irradiation has been developed. The methodology has been deployed for a wide range of heterocycles and electron-withdrawing & electron-donating groups. The protocol resulted in good to excellent yields under the given conditions (26 examples, 68–93% yield).

Graphical abstract: An expedient, efficient and solvent-free synthesis of T3P®-mediated amidation of benzhydrols with poorly reactive N-nucleophiles under MW irradiation

Supplementary files

Article information

Article type
Paper
Submitted
19 Sep 2021
Accepted
16 Jan 2022
First published
26 Jan 2022

New J. Chem., 2022,46, 4421-4426

An expedient, efficient and solvent-free synthesis of T3P®-mediated amidation of benzhydrols with poorly reactive N-nucleophiles under MW irradiation

S. Cheruku, S. C. Nagarakere, M. P. Sunilkumar, Y. Narayana, K. N. Manikyanally, K. S. Rangappa and K. Mantelingu, New J. Chem., 2022, 46, 4421 DOI: 10.1039/D1NJ04502D

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