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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534688Generated: October 30, 2026

Sulfur Dioxide → Sulfur Dioxide

https://huagongshe.com/reaction/534688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfur DioxideHCID 1119—
ReactantCesium fluorideHCID 25953—
ReactantSelectfluorHCID 2724933—
ReactantHCID 23727209HCID 23727209—
SolventAcetonitrileHCID 6342—
ProductSulfur DioxideHCID 1119—
ProductHCID 23726132HCID 23726132—

Reaction Steps

A solution of sulfur dioxide was prepared by bubbling sulfur dioxide (1.02 g, 16 mmol) in a solution of anhydrous acetonitrile (20 ml) at ambient temperature. This solution was added to PhSCF2CF2SiMe3 (8 mmol, prepared according to the procedure from example 2) and stirred at ambient temperature under an inert atmosphere. Anhydrous CsF (1.4 g, 9 mmol) was then added to the reaction mixture, which was stirred at ambient temperature overnight. The reaction was monitored by TLC and by 19F NMR (CDCl3) until the disappearance of PhSCF2CF2SiMe3. F-TEDA (2.9 g, 8.2 mmol) was added to the mixture, which was stirred for 1 h at ambient temperature. The mixture was concentrated and the solid residue washed with ethyl ether (10×50 ml). The filtrate was evaporated and the product purified by bulb-to-bulb distillation. The product 2-(phenylsulfanyl)-1,1,2,2-tetrafluoroethane-sulfonyl fluoride was obtained in the form of a colorless liquid (1.86 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853448B2
Source datasetuspto-grants-2014_10
ORD IDord-8b20835993fd47efbf37688bd8cb93d0
Source noteuspto-grants-2014_10