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.
Authors
- E. LEE
- Jongheon Jeong
- Solhye Choe (ORCID: https://orcid.org/0000-0002-9757-9295)
- Jun Hee Lee
Institutions
- Pohang University of Science and Technology (KR)
- Seoul National University (KR)
- Dongguk University (KR)
- Dongguk University WISE
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
- Field-Weighted Citation Impact
- 0.00