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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982499Generated: October 30, 2026

Pyridine → Pyridinium, 1-fluoro-, 1,1,1-trifluoromethanesulfonate (1:1)

https://huagongshe.com/reaction/982499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantFluorineHCID 24524—
ReactantSodium trifluoromethanesulfonateHCID 23676748—
SolventAcetonitrileHCID 6342—
ProductPyridinium, 1-fluoro-, 1,1,1-trifluoromethanesulfonate (1:1)HCID 272457671%

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a 100 ml anhydrous acetonitrile solution containing 10 g (0.126 mole) of pyridine a mixed gas of fluorine and nitrogen was introduced at a rate of 90 ml/min. at -40° C. under vigorous stirring. The amount of the fluorine gas introduced amounted to 0.18 mole. Subsequent to the fluorine introduction, 22 g (0.128 mole) of sodium trifluoromethanesulfonate as a XM reactant was added to the reaction solution after which the resultant reaction solution was maintained at -40° C. for 5 hours under stirring. Subsequently, the solvent, after filtering sodium fluoride, was distilled off and the resultant residue was recrystallized from methylene chloride to give 17.5 g (yield: 71%) of N-fluoropyridinium trifluoromethanesulfonate. The product thus obtained was repurified with methylene chloride/acetonitrile to recover 13.8 g (yield: 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04996320
Source datasetuspto-grants-1991_02
ORD IDord-ac517d2fd18b4c019af87d160ed2dbba
Source noteuspto-grants-1991_02