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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399959Generated: October 26, 2026

Chlorotrimethylsilane → Tris(4-tert-butoxyphenyl)sulfonium chloride

https://huagongshe.com/reaction/399959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Chloro-4-tert-butoxybenzeneHCID 140458—
ReactantMagnesiumHCID 5462224—
ReactantBis(4-tert-butoxyphenyl) sulfoxideHCID 15389810—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductTris(4-tert-butoxyphenyl)sulfonium chlorideHCID 8575909035%

Reaction Steps

A solution of 17.8 g (0.052 mol) of bis(4-tertbutoxyphenyl) sulfoxide in 52 g of THF was cooled on an ice bath. To the solution, 5.3 g (0.052 mol) of triethylamine was added and 14.1 g (0.13 mol) of trimethylsilyl chloride was dropwised at 0° to 10° C. Stirring was continued at 0 to 10° C. for 30 minutes. To this solution, a Grignard reagent which was conventionally prepared from 24.0 g (0.13 mol) of 4-tert-butoxychlorobenzene, 3.2 g (0.13 mol) of magnesium, and 40 g of THF was dropwised at 0° to 10° C. Stirring was continued at 0° to 10° C. for 30 minutes. 300 g of 20% ammonium chloride aqueous solution was added to the reaction mixture. To the organic layer was added 500 g of chloroform. The organic layer was washed twice with 200 g of water and the solvent was evaporated and residue was purifie by column chromatography (silica gel, eluent: chloroform/methanol), isolating 9.3 g (yield 35%) of tris(4-tert-butoxyphenyl)sulfonium chloride with 99% purity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05824824
Source datasetuspto-grants-1998_10
ORD IDord-e721bbc8b2e044319a53e787de2ae595
Source noteuspto-grants-1998_10