戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 233878作成日:2026年10月27日

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

https://huagongshe.com/reaction/233878

反応式

関与物質

役割名称HCID仕込み量
反応物p-BromoacetophenoneHCID 7466—
反応物Boron trifluoride etherateHCID 8000—
反応物1,3-PropanedithiolHCID 8013—
溶媒ChloroformHCID 6212—
溶媒DichloromethaneHCID 6344—
生成物4-Bromo-1-(1,3-dithian-2-yl)ethylbenzeneHCID 21960112—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05593995
出典データセットuspto-grants-1997_01
ORD IDord-02c6462e03d749fd9f284e5b88addf22
出典メモuspto-grants-1997_01