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HRID 362257作成日:2026年10月26日

1-(1-Benzofuran-3-yl)ethan-1-one → 1-(Benzofuran-3-yl)-2-bromoethanone

https://huagongshe.com/reaction/362257

反応式

関与物質

役割名称HCID仕込み量
反応物1-(1-Benzofuran-3-yl)ethan-1-oneHCID 11286612—
反応物Phenyltrimethylammonium bromide dibromideHCID 17977687—
溶媒TetrahydrofuranHCID 8028—
生成物1-(Benzofuran-3-yl)-2-bromoethanoneHCID 277658027.4%

反応手順

A solution of phenyltrimethylammonium tribromide (2.47 g) in tetrahydrofuran (20 ml) was added dropwise at ambient temperature under nitrogen over 5 minutes to a stirred solution of 3-acetylbenzo[b]furan (1 g) in tetrahydrofuran (20 ml), then the mixture was stirred at ambient temperature for a further 1.5 hours, filtered, and the solvent removed in vacuo. The residue was triturated with ether, and the resulting solid was collected by filtration and dried in vacuo at ambient temperature to give 3-(2-bromoacetyl)benzo[b]furan as an off-white solid (0.25 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05869492
出典データセットuspto-grants-1999_02
ORD IDord-10b5b665c38b46309fa8f6f6837d9876
出典メモuspto-grants-1999_02