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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359951Generated: October 26, 2026

Phenacyl bromide → Phenacyl phenyl sulfide

https://huagongshe.com/reaction/2359951

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 numberUS08686010B2
Source datasetuspto-grants-2014_04
ORD IDord-7252ab6c89104d44895ed05c28d497a9
Source noteuspto-grants-2014_04