Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Undecafluoropiperidine | HCID 136658 | — |
| Solvent | Hydrofluoric Acid | HCID 14917 | — |
| Product | Pyridine | HCID 1049 | 8% |
| Product | 2-Fluoropyridine | HCID 9746 | 13% |
Reaction Steps
Attention has recently been directed to using compounds of the N-F class, i.e., having an N-F bond, as electrophilic fluorinating agents. The prototypical member of this class is perfluoro-N-fluoropiperidine (R. E. Banks and G. E. Williamson, Chem. Ind. [London], 1964 and R. E. Banks, et al., J. Chem. Soc., Perkin Trans. I, [1972], 1098). However, this compound is obtainable only in low yields by electrochemical fluorination of either pyridine (about 8% yield) or 2-fluoropyridine (about 13%) in anhydrous hydrogen fluoride. Furthermore, this reagent is inadequately active in several applications, and, on transfer of fluorine to a carbanionic substrate, may liberate imidoyl fluoride perfluoro-1-azacyclohex-1-ene which then competes with the electrophilic fluorine source for the substrate. Similar problems militate against using analogous compounds such as perfluoro-(N-fluoro-2,6-dimethylpiperidine) and perfluoro-N-fluoromorpholine, (R. E. Banks, et al., J. Chem. Soc. Perkin Trans. I [1988], 2805) and poly[perfluoro-(N-fluoropiperidin-4-ylethylnene)](R. E. Banks, et al, J. Fluorine Chem., [1986], 34 281) as electrophilic fluorinating agents.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05233074 |
|---|
| Source dataset | uspto-grants-1993_08 |
|---|
| ORD ID | ord-3cc3d9ab509e47898f82c566ea024d83 |
|---|
| Source note | uspto-grants-1993_08 |
|---|