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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrichlorofluoromethaneHCID 6389—
ReactantFluorineHCID 24524—
ReactantSodium trifluoromethanesulfonateHCID 23676748—
SolventAcetonitrileHCID 6342—
ProductPyridinium, 1-fluoro-, 1,1,1-trifluoromethanesulfonate (1:1)HCID 272457667%

Reaction Conditions

Temperature-40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE035177
Source datasetuspto-grants-1996_03
ORD IDord-304a2f2fa32746b185593f50b81bda92
Source noteuspto-grants-1996_03