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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424330Generated: October 27, 2026

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

https://huagongshe.com/reaction/424330

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-tert-Butylphenyl)(diphenyl)sulfanium bromideHCID 22625536—
ReactantSodium 2-pivaloyloxy-1,1-difluoroethanesulfonateHCID 57817346—
SolventWaterHCID 962—
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 4-tert-butylphenyl-diphenylsulfonium bromide in water. The organic layer was separated and washed three times with 50 g of water. The organic layer was concentrated and diethyl ether was added to the residue for recrystallization. The target compound was obtained as white crystals, 26 g (yield 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08105748B2
Source datasetuspto-grants-2012_01
ORD IDord-b24592ffdb8f4c88848907ff02d28c6d
Source noteuspto-grants-2012_01