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HRID 717133作成日:2026年10月26日

p-Bromoacetophenone → 2-(4-Bromophenyl)propan-2-ol

https://huagongshe.com/reaction/717133

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HCID 178418573HCID 178418573—
溶媒TetrahydrofuranHCID 8028—
生成物2-(4-Bromophenyl)propan-2-olHCID 1268192099.4%

反応条件

温度-50 °C

反応手順

1-(4-Bromophenyl)ethanone (9.25 g, 46.5 mmol) was dissolved in tetrahydrofuran (200 mL). The solution was cooled in a −50° C. bath. Methylmagnesium bromide (3M in ether, 46.5 mL, 139 mmol) was added over a 15 min period. The reaction was allowed to warm to room temperature and then stirred for 20 h. The reaction was quenched with saturated ammonium chloride and then extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, filtered and concentrated to give an oil. The oil was purified on a silica gel column (0-20% ethyl acetate in hexanes) to give the product a colorless oil (9.1 g, 46.2 mmol, 91% yield). MS (ESI) m/z 197.1 [M]+, 199.1 [M+2]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09193692B2
出典データセットuspto-grants-2015_11
ORD IDord-86522330519141088ca8b4867b553901
出典メモuspto-grants-2015_11