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.
Authors
- Toshiki Tajima (ORCID: https://orcid.org/0009-0000-8933-1225)
- Haruka Homma (ORCID: https://orcid.org/0009-0005-0854-5261)
Institutions
- Shibaura Institute of Technology (JP)
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
- 0.00