Catalytic Appel fluorination of alcohols with potassium fluoride

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Authors: Anirban Mondal, Job J. C. Struijs, Caleb J. N. Doyle, Zijun Chen, Zian Wang, Worawit Tangamornchaipattana, Christophe Allais, Paul Richardson, Jared L. Piper, Robert S. Paton, Simon Aldridge, Véronique Gouverneur
Cited by: 1
References: 106

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.

Fields of Study & Subjects

Fluorine in Organic Chemistry Advanced Synthetic Organic Chemistry Catalytic Cross-Coupling Reactions

Publication details

Journal / source
Science
Publisher
American Association for the Advancement of Science (AAAS)
Volume
393
Issue
6810
Pages
514–521
Publication date
30 July 2026
Language
EN