Heterogeneous Iron-Catalyzed Borylation of Aryl Fluorides

We report a mild and practical iron-catalyzed protocol for the borylation of aryl fluorides using commercially available FeCl<sub>3</sub>, a β-diketiminate ligand, and HBpin as a boron source. The method exhibits broad substrate scope with excellent yields (up to 99%), including non-π-extended fluoroarenes, heterocycles, and substrates with unprotected phenolic OH groups, operating efficiently under ambient to elevated temperatures. Comprehensive mechanistic studies reveal that the reaction proceeds via in situ formation of Grignard intermediates and iron nanoparticles, establishing a heterogeneous catalytic pathway distinct from previous homogeneous systems. This protocol offers a cost-effective, atom-economical route to arylboronates using earth-abundant metal catalysis, significantly expanding the synthetic utility of C-F bond functionalization under mild conditions.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-02-04
DOI
https://doi.org/10.1021/acs.joc.5c02752
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
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article

Heterogeneous Iron-Catalyzed Borylation of Aryl Fluorides

E. LEE, Jongheon Jeong, Solhye Choe, Jun Hee Lee
The Journal of Organic Chemistry
Catalytic Cross-Coupling Reactions
article

Heterogeneous Iron-Catalyzed Borylation of Aryl Fluorides

E. LEE, Jongheon Jeong, Solhye Choe, Jun Hee Lee
article en

Abstract

We report a mild and practical iron-catalyzed protocol for the borylation of aryl fluorides using commercially available FeCl<sub>3</sub>, a β-diketiminate ligand, and HBpin as a boron source. The method exhibits broad substrate scope with excellent yields (up to 99%), including non-π-extended fluoroarenes, heterocycles, and substrates with unprotected phenolic OH groups, operating efficiently under ambient to elevated temperatures. Comprehensive mechanistic studies reveal that the reaction proceeds via in situ formation of Grignard intermediates and iron nanoparticles, establishing a heterogeneous catalytic pathway distinct from previous homogeneous systems. This protocol offers a cost-effective, atom-economical route to arylboronates using earth-abundant metal catalysis, significantly expanding the synthetic utility of C-F bond functionalization under mild conditions.

The Journal of Organic ChemistryVol. 91(7)
Pohang University of Science and Technology (KR), Seoul National University (KR), Dongguk University (KR), Dongguk University WISE
Openalex Percentile: Top 66%
Catalytic Cross-Coupling Reactions
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Heterogeneous Iron-Catalyzed Borylation of Aryl Fluorides — E. LEE, Jongheon Jeong, et al. · The Journal of Organic Chemistry (2026) | TGRS Research Map | TGRS