戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2183655作成日:2026年10月27日

Phenyltrimethylammonium bromide dibromide → 1-(Benzo[b]thiophen-7-yl)-2-bromopropan-1-one

https://huagongshe.com/reaction/2183655

反応式

関与物質

役割名称HCID仕込み量
反応物Phenyltrimethylammonium bromide dibromideHCID 17977687—
反応物1-(Benzo[b]thiophen-7-yl)propan-1-oneHCID 22473897—
溶媒TetrahydrofuranHCID 8028—
生成物1-(Benzo[b]thiophen-7-yl)-2-bromopropan-1-oneHCID 22474143112.5%

反応手順

Phenyltrimethylammonium tribromide (1.52 g) was added in portions under nitrogen at 0° C. over 30 minutes to a stirred solution of 1-(benzo[b]thiophen-7-yl)propan-1-one (0.77 g) in tetrahydrofuran (110 ml), then the mixture was stirred at ambient temperature for 18 hours. Further phenyltrimethylammonium tribromide (0.76 g) was added and the mixture was heated under reflux for 4 hours. Further phenyltrimethylammonium tribromide (0.76 g) was added, then the mixture was heated under reflux for 90 minutes, cooled to ambient temperature and filtered. The solvent was removed in vacuo and the residue was purified by flash chromatography over silica using a 7:3 mixture of petroleum ether (b.p. 60-80° C.) and dichloromethane as eluant. Appropriate fractions were combined and the solvents removed in vacuo to give 1-(benzo[b]thiophen-7-yl)-2-bromopropan-1-one (0.71 g) as an oil which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06900216B2
出典データセットuspto-grants-2005_05
ORD IDord-8f8daf008bb5407a9b9d5c9062fb3418
出典メモuspto-grants-2005_05