Visible-Light Photoredox-Induced and Copper-Catalyzed Trifluoromethoxylation of Diaryliodonium Tetrafluoroborates

A light-induced and copper-catalyzed trifluoromethoxylation reaction of aryl iodonium tetrafluoroborates was reported. This scalable protocol demonstrates broad functional group compatibility and offers a practical and efficient strategy for the introduction of the trifluoromethoxy group into aromatic systems. Furthermore, mechanistic studies suggested that aryl radicals are generated via visible-light catalysis during the reaction.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-02-05
DOI
https://doi.org/10.1021/acs.joc.5c03177
Primary Topic
Fluorine in Organic Chemistry
Type
article
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article

Visible-Light Photoredox-Induced and Copper-Catalyzed Trifluoromethoxylation of Diaryliodonium Tetrafluoroborates

Mingxin Zhao, Qingyun Huang, Pingping Tang, Jinjin Li
The Journal of Organic Chemistry
Fluorine in Organic Chemistry
article

Visible-Light Photoredox-Induced and Copper-Catalyzed Trifluoromethoxylation of Diaryliodonium Tetrafluoroborates

Mingxin Zhao, Qingyun Huang, Pingping Tang, Jinjin Li
article en

Abstract

A light-induced and copper-catalyzed trifluoromethoxylation reaction of aryl iodonium tetrafluoroborates was reported. This scalable protocol demonstrates broad functional group compatibility and offers a practical and efficient strategy for the introduction of the trifluoromethoxy group into aromatic systems. Furthermore, mechanistic studies suggested that aryl radicals are generated via visible-light catalysis during the reaction.

The Journal of Organic ChemistryVol. 91(7)
Nankai University (CN)
Clean water and sanitation
Openalex Percentile: Top 64%
Fluorine in Organic Chemistry
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