Heterobenzyl Chlorides as Linchpins for C–H Arylation via Sequential C–H Chlorination/Cross-Electrophile Coupling

Synthetic methods that use C-(sp<sup>3</sup>)-H bonds in carbon-carbon cross-coupling reactions are limited and often lack generality, particularly with substrates containing basic heterocycles. Here, we demonstrate the arylation of heterobenzylic C-H bonds by using heterobenzyl chlorides as linchpins that can undergo Ni-catalyzed cross-electrophile coupling with aryl iodides. The results show different reactivity for primary and secondary heterobenzyl chlorides and also show differences among secondary heterobenzyl chlorides at different positions on the heteroaromatic ring. The Ni-catalyzed conditions identified for each of these substrate classes ensure that the rate of heterobenzyl chloride activation complements the rate of aryl iodide activation. These methods are demonstrated with series of heterobenzyl chlorides and (hetero)-aryl iodides, providing a general strategy for C-(sp<sup>3</sup>)-H arylation.

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Journal
ACS Catalysis
Published
2026-02-03
DOI
https://doi.org/10.1021/acscatal.5c08221
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
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article

Heterobenzyl Chlorides as Linchpins for C–H Arylation via Sequential C–H Chlorination/Cross-Electrophile Coupling

Nicole C. Goodwin, Luana Cardinale, Darren L. Poole, Allison R. Dick et al.
ACS Catalysis
Catalytic C–H Functionalization Methods
article

Heterobenzyl Chlorides as Linchpins for C–H Arylation via Sequential C–H Chlorination/Cross-Electrophile Coupling

Nicole C. Goodwin, Luana Cardinale, Darren L. Poole, Allison R. Dick, Shannon S. Stahl, Marco A. Lopez, Jack T. Floreancig
article en

Abstract

Synthetic methods that use C-(sp<sup>3</sup>)-H bonds in carbon-carbon cross-coupling reactions are limited and often lack generality, particularly with substrates containing basic heterocycles. Here, we demonstrate the arylation of heterobenzylic C-H bonds by using heterobenzyl chlorides as linchpins that can undergo Ni-catalyzed cross-electrophile coupling with aryl iodides. The results show different reactivity for primary and secondary heterobenzyl chlorides and also show differences among secondary heterobenzyl chlorides at different positions on the heteroaromatic ring. The Ni-catalyzed conditions identified for each of these substrate classes ensure that the rate of heterobenzyl chloride activation complements the rate of aryl iodide activation. These methods are demonstrated with series of heterobenzyl chlorides and (hetero)-aryl iodides, providing a general strategy for C-(sp<sup>3</sup>)-H arylation.

ACS CatalysisVol. 16(4)
University of Wisconsin–Madison (US), South College (US), Metabolic Technologies (United States) (US), GlaxoSmithKline (Croatia) (HR), Wheaton College - Illinois (US)
Openalex Percentile: Top 68%
Catalytic C–H Functionalization Methods
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Heterobenzyl Chlorides as Linchpins for C–H Arylation via Sequential C–H Chlorination/Cross-Electrophile Coupling — Nicole C. Goodwin, Luana Cardinale, et al. · ACS Catalysis (2026) | TGRS Research Map | TGRS