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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182010Generated: October 30, 2026

Triphenylsulfonium chloride → HCID 21863778, compound

https://huagongshe.com/reaction/1182010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylsulfonium chlorideHCID 61343—
ReactantHCID 59514422HCID 59514422—
SolventWaterHCID 962—
ProductHCID 21863778HCID 21863778—

Reaction Steps

An eggplant-shaped flask was charged with a solution of 20 g of triphenylsulfonium chloride in 500 ml of water. A separately prepared solution of 20 g of sodium 1,1,2,2-tetrafluoro-2-(norbornan-2-yl)ethanesulfonate in 500 ml of water was added dropwise to the solution at room temperature. The mixture was stirred for 30 minutes. The reaction solution was extracted with ethyl acetate. The organic layer was washed with water twice and distilled under reduced pressure to obtain colorless highly viscous oil of triphenylsulfonium 1,1,2,2-tetrafluoro-2-(norbornan-2-yl)ethanesulfonate of the following formula (34) (yield 43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288359B2
Source datasetuspto-grants-2007_10
ORD IDord-0b71ce98be5c4c2b97ce7d4750ca392a
Source noteuspto-grants-2007_10