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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670878Generated: October 27, 2026

Phenacyl bromide → Phenacyl phenyl sulfide

https://huagongshe.com/reaction/1670878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantThiophenolHCID 7969—
ReactantPotassium CarbonateHCID 11430—
SolventEthanolHCID 702—
ProductPhenacyl phenyl sulfideHCID 8533898%

Reaction Steps

To a suspension of 2-bromoacetophenone (10 g) and potassium carbonate (7.1 g) in ethanol (150 mL) was added thiophenol (5.2 mL) under ice-cooling, and the mixture was stirred at room temperature for 12 hr. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogen carbonate solution, water and saturated brine in this order, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent:hexane-ethyl acetate=15:1) to give the title compound as yellow crystals (yield 11 g, 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994205B2
Source datasetuspto-grants-2011_08
ORD IDord-c587b3e779f0497bab4237cfb254a227
Source noteuspto-grants-2011_08