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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 55628Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/55628

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-BromoacetophenoneHCID 7466—
EduktBoron trifluoride etherateHCID 8000—
Edukt1,3-PropanedithiolHCID 8013—
LösungsmittelChloroformHCID 6212—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Bromo-1-(1,3-dithian-2-yl)ethylbenzeneHCID 21960112—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05624927
Quelldatensatzuspto-grants-1997_04
ORD IDord-6cb87811cba8461b8d090235ec7639ac
Quellennotizuspto-grants-1997_04