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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70581Generated: October 26, 2026

Water → {3-[(4-Bromophenyl)sulfanyl]propoxy}(tert-butyl)dimethylsilane

https://huagongshe.com/reaction/70581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant4-BromothiophenolHCID 66049—
Reactant(3-Bromopropoxy)(tert-butyl)dimethylsilaneHCID 607486—
SolventDimethylformamideHCID 6228—
Product{3-[(4-Bromophenyl)sulfanyl]propoxy}(tert-butyl)dimethylsilaneHCID 5845278395.9%

Reaction Steps

Potassium carbonate (4.1 g) and (3-bromopropoxy)-tert-butyldimethylsilane (4.1 g) were added to a solution of 4-bromothiophenol (3.0 g) in N,N-dimethylformamide, and the mixture was stirred at room temperature overnight. The reaction solution was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and filtered. The solvent was then evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=50:1→20:1) to give the title compound as a colorless oil (5.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822503B2
Source datasetuspto-grants-2014_09
ORD IDord-89f6114bf4d848c3aab847590a690aff
Source noteuspto-grants-2014_09