Copper-Catalyzed Cross-Coupling of Malonates with Aryl Halides Using Hydroxypicolinamide Ligands

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Authors: Ian Hotham, Daniel W. Widlicka
Cited by: 1
References: 28

Abstract

Abstract Cu-catalyzed cross-coupling of aryl halides and malonates using hydroxypicolinamide ligands to furnish the corresponding aryl malonates is disclosed herein. Malonates are commonly coupled with aryl halides via Pd catalysis, with a few reports of classic Hurtley-type Cu-mediated couplings. The Cu-MPBS system, originally designed for C–N coupling, has been further developed for the Cu-catalyzed coupling of diethyl malonate with aryl bromides and less precedented aryl chlorides. Our hydroxypicolinamide ligand scaffold promotes the Hurtley-type coupling of diethyl malonate under mild conditions for aryl bromides (20–40 °C) and aryl chlorides (60–80 °C) with low Cu loading (2–4 mol %). Reaction conditions are compatible with a wide variety of functional groups and heterocycles to provide the desired malonate. Furthermore, we demonstrated a telescoped process to the α-aryl ester simply by heating to drive subsequent decarboxylation.

Fields of Study & Subjects

Catalytic Cross-Coupling Reactions Catalytic C–H Functionalization Methods Sulfur-Based Synthesis Techniques

Publication details

Journal / source
Organic Process Research & Development
Publisher
American Chemical Society (ACS)
Volume
30
Issue
10
Pages
2735-2742
Publication date
20 July 2026
Language
EN