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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670361Generated: November 1, 2026

(4-tert-Butylphenyl)(diphenyl)sulfanium bromide → 4-Tert-butylphenyldiphenylsulfonium 2-pivaloyloxy-1,1-difluoroethanesulfonate

https://huagongshe.com/reaction/1670361

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-tert-Butylphenyl)(diphenyl)sulfanium bromideHCID 22625536—
ReactantSodium 2-pivaloyloxy-1,1-difluoroethanesulfonateHCID 57817346—
SolventDichloromethaneHCID 6344—
Product4-Tert-butylphenyldiphenylsulfonium 2-pivaloyloxy-1,1-difluoroethanesulfonateHCID 8663275479%

Reaction Steps

In 150 g of dichloromethane were dissolved 20 g (0.052 mole) of sodium 2-(pivaloyloxy)-1,1-difluoroethanesulfonate (purity 70%) and 217 g (0.052 mole) of a 4-tert-butylphenyl-diphenylsulfonium bromide aqueous solution. The organic layer was separated, washed three times with 50 g of water, and concentrated. Diethyl ether was added to the residue for recrystallization, obtaining the target compound as white crystals. 26 g (yield 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07993811B2
Source datasetuspto-grants-2011_08
ORD IDord-30f48d88c7f94e4d99afc711a802c59c
Source noteuspto-grants-2011_08