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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753669Generated: October 28, 2026

Dichloromethane → Bis(4-tert-butylphenyl)(4-fluorophenyl)-sulfonium 1,1,3,3,3-pentafluoro-2-hydroxypropane-1-sulfonate

https://huagongshe.com/reaction/1753669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBenzyltrimethylammonium 1,1,3,3,3-pentafluoro-2-hydroxypropane-1-sulfonateHCID 86664292—
ReactantBis[4-(tert-butyl)phenyl](4-fluorophenyl)sulfonium bromideHCID 131733658—
SolventWaterHCID 962—
ProductBis(4-tert-butylphenyl)(4-fluorophenyl)-sulfonium 1,1,3,3,3-pentafluoro-2-hydroxypropane-1-sulfonateHCID 13173365981.5%

Reaction Steps

A mixture of 13 g of benzyltrimethylammonium 1,1,3,3,3-pentafluoro-2-hydroxypropane-1-sulfonate synthesized according to the method of JP-A 2012-107151, 14 g of bis(4-tert-butylphenyl)(4-fluorophenyl)sulfonium bromide obtained in Synthesis Example 1-3, 70 g of methylene chloride, and 30 g of deionized water was stirred for 30 minutes. The organic layer was separated, washed with water, and concentrated in vacuum. MIBK (100 g) was added to the concentrate, followed by vacuum concentration again. The residue was dissolved in methanol, after which diisopropyl ether was added for recrystallization. The resulting crystals were collected by filtration and dried in vacuum, obtaining 15 g of the target compound, bis(4-tert-butylphenyl)(4-fluorophenyl)sulfonium 1,1,3,3,3-pentafluoro-2-hydroxypropane-1-sulfonate as white crystals. Yield 80%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09164384B2
Source datasetuspto-grants-2015_10
ORD IDord-ab19bb1931ad459985d4cb853e471337
Source noteuspto-grants-2015_10