HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440171Generated: October 30, 2026
Pyridine → Pyridinium, 1-fluoro-, 1,1,1-trifluoromethanesulfonate (1:1)
https://huagongshe.com/reaction/1440171
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trichlorofluoromethane | HCID 6389 | — |
| Reactant | Fluorine | HCID 24524 | — |
| Reactant | Sodium trifluoromethanesulfonate | HCID 23676748 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Pyridinium, 1-fluoro-, 1,1,1-trifluoromethanesulfonate (1:1) | HCID 2724576 | 67% |
Reaction Steps
To a 50 ml trichlorofluoromethane solution containing 1.0 g (12.6 m moles) of pyridine a mixed gas of fluorine and nitrogen in a volumetric ratio of 1:9 was introduced at a rate of 30 ml/min. at -78° C. under vigorous stirring. The amount of the fluorine gas introduced amounted to 34.8 mmoles. Subsequent to the fluorine introduction, 20 ml of anhydrous acetonitrile and 2.2 g (12.8 mmoles) of sodium trifluoro-methanesulfonate as a XM reactant were added to the reaction solution after which the temperature of the solution was raised to -40° C., while removing the solvent with the aid of an aspirator. The solvent, after filtering sodium fluoride formed as a byproduct, was distilled off and the resultant residue was recrystallized from THF to give 1.75 g (yield: 67%) of N-fluoropyridinium trifluoromethanesulfonate, the physical properties of which are shown in Table 6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE035177 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-304a2f2fa32746b185593f50b81bda92 |
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| Source note | uspto-grants-1996_03 |
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