Direct Trifluoromethylation and Chlorodifluoromethylation Enabled by the Reaction of Reformatsky Reagent with YlideFluor

A general method for the direct trifluoromethylation and chlorodifluoromethylation of Reformatsky reagents derived from various amides or ketones using YlideFluor or YlideFluor-CF<sub>2</sub>Cl was described. This reaction proceeds under mild conditions and exhibits a broad functional group tolerance. The utility of this protocol was demonstrated through the synthesis of trifluoromethylated derivatives of two pharmaceutical agents, donepezil and ibudilast.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-02-05
DOI
https://doi.org/10.1021/acs.joc.5c03015
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.00
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article

Direct Trifluoromethylation and Chlorodifluoromethylation Enabled by the Reaction of Reformatsky Reagent with YlideFluor

Qilong Shen, Lingpu Meng, Wenju Wan
The Journal of Organic Chemistry
Fluorine in Organic Chemistry
article

Direct Trifluoromethylation and Chlorodifluoromethylation Enabled by the Reaction of Reformatsky Reagent with YlideFluor

Qilong Shen, Lingpu Meng, Wenju Wan
article en

Abstract

A general method for the direct trifluoromethylation and chlorodifluoromethylation of Reformatsky reagents derived from various amides or ketones using YlideFluor or YlideFluor-CF<sub>2</sub>Cl was described. This reaction proceeds under mild conditions and exhibits a broad functional group tolerance. The utility of this protocol was demonstrated through the synthesis of trifluoromethylated derivatives of two pharmaceutical agents, donepezil and ibudilast.

The Journal of Organic ChemistryVol. 91(7)
Henan University of Technology (CN), Shanghai Institute of Organic Chemistry (CN), University of Chinese Academy of Sciences (CN)
Clean water and sanitation
Openalex Percentile: Top 65%
Fluorine in Organic Chemistry
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