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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184536Generated: November 1, 2026

p-Bromoacetophenone → 4-Bromo-1-(1,3-dithian-2-yl)ethylbenzene

https://huagongshe.com/reaction/2184536

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromoacetophenoneHCID 7466—
ReactantBoron trifluoride etherateHCID 8000—
Reactant1,3-PropanedithiolHCID 8013—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product4-Bromo-1-(1,3-dithian-2-yl)ethylbenzeneHCID 21960112—

Reaction Steps

To the compound p-bromoacetophenone (36.85 g, 185 mmol) in trichloromethane (300 ml) was added 1,3-propanedithiol (25 g, 230 mmol) and boron trifluoride etherate (3 ml). The resulting mixture was stirred at room temperature for 48 hours. The mixture was diluted with dichloromethane (500 ml), washed twice with 10% sodium hydroxide (200 ml), water, and brine, and then dried (Na2SO4). The product was concentrated to an oil. A portion was stirred with ether (100 ml) and a crystalline product was formed. The crystalline product was recovered by filtration and purified by recrystallization to yield 4-bromo-1-(1,3-dithian-2-yl)ethylbenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037729E1
Source datasetuspto-grants-2002_06
ORD IDord-dee2acf5d04444fcb5607aa6c77d3241
Source noteuspto-grants-2002_06