Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394577Generated: October 29, 2026

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

https://huagongshe.com/reaction/2394577

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 numberUS05811430
Source datasetuspto-grants-1998_09
ORD IDord-5161979ebc7d4c0482e436dd7f2d2323
Source noteuspto-grants-1998_09