Catalytic Appel fluorination of alcohols with potassium fluoride

Appel halogenation reactions are widely used to convert alcohols to alkyl halides but are not suitable to prepare alkyl fluorides because fluoride is sequestered as a difluorophosphorane. In this work, we introduce bench-stable neopentoxyphosphonium salts to solve this enduring challenge. With these reagents, various alcohols undergo fluorination with potassium fluoride under hydrogen bonding phase-transfer catalysis, a manifold offering a pathway to enantioselective fluorination of alcohols. Mechanistically, a neopentoxyfluorophosphorane is formed, which undergoes reversible exchange with the alcohol substrate in preference to difluorophosphorane formation. The catalyst assists with potassium fluoride solubilization and with phosphorus-fluorine bond dissociation, leading to the alkoxyphosphonium fluoride ion pair undergoing stereoinvertive fluorination. Turnover results from stronger binding of the catalyst to fluoride than phosphine oxide, the by-product of the reaction, which is recyclable as starting material for the synthesis of the phosphonium reagents.

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Publication Details

Journal
Science
Published
2026-07-30
DOI
https://doi.org/10.1126/science.aec6298
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Catalytic Appel fluorination of alcohols with potassium fluoride

Paul Richardson, Simon Aldridge, Job J. C. Struijs, Robert S. Paton et al.
Science
Fluorine in Organic Chemistry
article

Catalytic Appel fluorination of alcohols with potassium fluoride

Paul Richardson, Simon Aldridge, Job J. C. Struijs, Robert S. Paton, Christophe Allais, Véronique Gouverneur, Jared L. Piper, Anirban Mondal, Worawit Tangamornchaipattana, Zian Wang, Zijun Chen, Caleb J. N. Doyle
article en

Abstract

Appel halogenation reactions are widely used to convert alcohols to alkyl halides but are not suitable to prepare alkyl fluorides because fluoride is sequestered as a difluorophosphorane. In this work, we introduce bench-stable neopentoxyphosphonium salts to solve this enduring challenge. With these reagents, various alcohols undergo fluorination with potassium fluoride under hydrogen bonding phase-transfer catalysis, a manifold offering a pathway to enantioselective fluorination of alcohols. Mechanistically, a neopentoxyfluorophosphorane is formed, which undergoes reversible exchange with the alcohol substrate in preference to difluorophosphorane formation. The catalyst assists with potassium fluoride solubilization and with phosphorus-fluorine bond dissociation, leading to the alkoxyphosphonium fluoride ion pair undergoing stereoinvertive fluorination. Turnover results from stronger binding of the catalyst to fluoride than phosphine oxide, the by-product of the reaction, which is recyclable as starting material for the synthesis of the phosphonium reagents.

ScienceVol. 393(6810)
Pfizer (United States) (US), University of Oxford (GB), Colorado State University (US)
National Science Foundation, Pfizer, UK Research and Innovation, Clarendon Fund, H2020 European Research Council, HORIZON EUROPE Marie Sklodowska-Curie Actions
Clean water and sanitation
Openalex Percentile: Top 11%
Fluorine in Organic Chemistry
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