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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415682Generated: October 26, 2026

Phenacyl bromide → Phenacyl phenyl sulfide

https://huagongshe.com/reaction/1415682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
ReactantThiophenolHCID 7969—
SolventPyridineHCID 1049—
ProductPhenacyl phenyl sulfideHCID 8533867.7%

Reaction Steps

To 300 mL of pyridine was added a-bromoacetophenone (150 g, 750 mmol) and thiophenol (83 g, 750 mmol). The mixture was heated at reflux for six hours. The pyridine was evaporated and the residue dissolved in ethyl acetate. The ethyl acetate solution was washed exhaustively with 1 N sodium hydroxide, then with 1 N hydrochloric acid, dried over magnesium sulfate, filtered, and evaporated to yield a brown oil. The product was crystallized from ethanol at 0° C. to yield 116 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05908859
Source datasetuspto-grants-1999_06
ORD IDord-a2d7cc1c6e9c4a04b436aa176967140e
Source noteuspto-grants-1999_06