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HRID 42300作成日:2026年10月25日

Hexane → 2-Bromo-1-(2-phenoxypyrimidin-5-yl)ethanone

https://huagongshe.com/reaction/42300

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物Tetra-n-butylammonium tribromideHCID 23500184—
反応物1-(2-Phenoxypyrimidin-5-yl)ethanoneHCID 59252440—
溶媒DichloromethaneHCID 6344—
生成物2-Bromo-1-(2-phenoxypyrimidin-5-yl)ethanoneHCID 5925242668.4%

反応条件

温度40 °C

反応手順

To a solution consisting of 1-(2-phenoxypyrimidin-5-yl)ethanone (Step B, 400 mg, 1.87 mmol) in dichloromethane (14 mL) was added tetrabutylammonium tribromide (990 mg, 2.05 mmol). The reaction mixture was sealed with a screw top and warmed at 40° C. overnight and allowed to cool to room temperature. Hexane (4 mL) was subsequently added. After three hours and little precipitation, additional (150 mg) tetrabutylammonium tribromide was added and the reaction mixture was stirred overnight at room temperature. The pale yellow precipitate that formed was collected on a filter and washed with 1:1 dichloromethane-hexane to afford the title intermediate (375 mg, 68%); Rf 0.43 with 3:1 v/v hexanes-ethyl acetate; MS (ESI+) m/z 295, 293 (M+1, Br isotopes).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536185B2
出典データセットuspto-grants-2013_09
ORD IDord-394bb218ce9a406696585bd4e93d8732
出典メモuspto-grants-2013_09