Synthesis of novel nucleophilic fluorinating reagents derived from KF

Abstract We present safe, convenient methods for synthesizing nucleophilic fluorinating reagents—specifically amine-3HF and R4NF(HFIP)3 complexes—using KF as a sustainable fluorine source. Cation exchange between KF and Amberlyst 15DRY generates HF in situ, enabling the efficient synthesis of various amine-3HF complexes. Alternatively, ion exchange between KF and R4NBr in an HFIP/CH2Cl2 co-solvent system provides a straightforward route to R4NF(HFIP)3 complexes. This review outlines the theoretical background, synthetic strategies, achievements, and future prospects of these KF-derived reagents.

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Publication Details

Journal
Chemistry Letters
Published
2026-05-30
DOI
https://doi.org/10.1093/chemle/upag105
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
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article

Synthesis of novel nucleophilic fluorinating reagents derived from KF

Toshiki Tajima, Haruka Homma
Chemistry Letters
Fluorine in Organic Chemistry
article

Synthesis of novel nucleophilic fluorinating reagents derived from KF

Toshiki Tajima, Haruka Homma
article en

Abstract

Abstract We present safe, convenient methods for synthesizing nucleophilic fluorinating reagents—specifically amine-3HF and R4NF(HFIP)3 complexes—using KF as a sustainable fluorine source. Cation exchange between KF and Amberlyst 15DRY generates HF in situ, enabling the efficient synthesis of various amine-3HF complexes. Alternatively, ion exchange between KF and R4NBr in an HFIP/CH2Cl2 co-solvent system provides a straightforward route to R4NF(HFIP)3 complexes. This review outlines the theoretical background, synthetic strategies, achievements, and future prospects of these KF-derived reagents.

Chemistry Letters
Shibaura Institute of Technology (JP)
Responsible consumption and production
Openalex Percentile: Top 7%
Fluorine in Organic Chemistry
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