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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492710Generated: October 31, 2026

Acetonitrile → 1-Fluoro-4,6-bis(trifluoromethyl)pyridin-1-ium-2-sulfonate

https://huagongshe.com/reaction/1492710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantFluorineHCID 24524—
ReactantHCID 10685264HCID 10685264—
SolventDiethyl EtherHCID 3283—
Product1-Fluoro-4,6-bis(trifluoromethyl)pyridin-1-ium-2-sulfonateHCID 2737291—

Reaction Steps

In a 25 ml flask, acetonitrile (6 ml) was added to 4,6-bistrifluoromethylpyridine-2-sulfonic acid (874 mg, 2.64 mmol) to prepare a homogeneous mixture. Then, the flask was dipped in a cooling bath kept at -40° C., and to the mixture, the fluorine gas diluted with the nitrogen gas to a concentration of 10% was introduced at a flow rate of 15 ml/min. The total amount of the fluorine gas was 211 ml. As the fluorination reaction proceeded, a precipitate was formed. After the reaction, only the nitrogen gas was introduced for 30 minutes. After the addition of ethyl ether to the mixture, the resulting precipitate was recovered by filtration to obtain N-fluoro-4,6-bistrifluoromethylpyridinium-2-sulfonate (787 mg). Yield, 95%. Melting point, 172°-174° C. (with decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05374732
Source datasetuspto-grants-1994_12
ORD IDord-7b784b179a35487cb0dc1e662425932b
Source noteuspto-grants-1994_12