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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088299Generated: November 1, 2026

Triphenylsulfonium chloride → HCID 86638824, compound

https://huagongshe.com/reaction/2088299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylsulfonium chlorideHCID 61343—
ReactantHCID 59185162HCID 59185162—
SolventWaterHCID 962—
ProductHCID 86638824HCID 8663882464%

Reaction Steps

A 100 mL reactor was charged with 3.0 g (purity 26%, 2.9 millimoles) of sodium 2-valeryloxy-1,1-difluoroethanesulfonate and 30 g of water, followed by adding dropwise an aqueous solution of triphenylsulfonium chloride [17.8 g (5.2 millimoles/1.8 equivalents) of triphenylsulfonium chloride and 16.2 g of water] at room temperature, followed by stirring at room temperature for 1.5 hours. Then, extraction was conducted by adding 30 mL of chloroform. The obtained organic layer was washed two times with water, followed by distilling solvent off, thereby obtaining 0.96 g of the target triphenylsulfonium 2-valeryloxy-1,1-difluoroethanesulfonate. Upon this, purity was 98%, and yield was 64%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08435717B2
Source datasetuspto-grants-2013_05
ORD IDord-252743217c8d4110ac6cb104b20895cc
Source noteuspto-grants-2013_05