Issue 30, 2024, Issue in Progress

Recyclable LaF3·Pd nanocatalyst in Suzuki coupling: green synthesis of biaryls from haloarenes and phenylboronic acids

Abstract

Herein we prepared the novel LaF3·Pd nanocatalyst characterized by XRD and TEM analysis. The nanocatalyst was applied in Suzuki coupling reaction for the synthesis of biaryls in aqueous medium from readily available aryl halides (bromides and iodides) and substituted phenylboronic acids in the presence of K2CO3 as the base at 70 °C. The present method is capable of giving the C–C coupled product in good to excellent yields (up to 97%). The reactions were conducted under green conditions in aqueous medium and the nanocatalyst used in this study was recyclable. The recyclability and reusability of the catalyst was checked for seven consecutive cycles without significant loss in reactivity.

Graphical abstract: Recyclable LaF3·Pd nanocatalyst in Suzuki coupling: green synthesis of biaryls from haloarenes and phenylboronic acids

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Article information

Article type
Paper
Submitted
26 Jan 2024
Accepted
13 Jun 2024
First published
05 Jul 2024
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2024,14, 21269-21276

Recyclable LaF3·Pd nanocatalyst in Suzuki coupling: green synthesis of biaryls from haloarenes and phenylboronic acids

S. Panda, S. Patra, S. S. Acharya, G. Phaomei and B. B. Parida, RSC Adv., 2024, 14, 21269 DOI: 10.1039/D4RA00686K

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