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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640375Generated: October 30, 2026

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

https://huagongshe.com/reaction/1640375

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 an aqueous solution of 4-tert-butylphenyldiphenylsulfonium bromide. The organic layer was separated and washed with 50 g of water three times. 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 numberUS08114571B2
Source datasetuspto-grants-2012_02
ORD IDord-ac38d62b52ff43b4a1b7cb332feccfbc
Source noteuspto-grants-2012_02