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HRID 62783作成日:2026年10月25日

Cyclopentanone → 1-(2-(Trifluoromethyl)phenyl)cyclopentanol

https://huagongshe.com/reaction/62783

反応式

関与物質

役割名称HCID仕込み量
反応物CyclopentanoneHCID 8452—
反応物Benzene, 1-bromo-2-(trifluoromethyl)-HCID 9806—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物1-(2-(Trifluoromethyl)phenyl)cyclopentanolHCID 6280214048.9%

反応条件

温度-78 °C

反応手順

A solution of 1-bromo-2-(trifluoromethyl)benzene (0.5 g, 2.222 mmol) in anhydrous THF (10 mL) was cooled to −78° C. (dry ice IPA bath) under argon atmosphere. BuLi (2.5 M in hexanes, 1.068 mL, 2.67 mmol) was added in drops with efficient stirring. The reaction mixture was stirred at −78° C. for 40 min. A solution of cyclopentanone (0.243 g, 2.89 mmol) in anhydrous THF (1.5 mL) was added slowly (in drops) at −78° C. The reaction mixture was stirred at −78° C. for 30 min, gradually brought to room temperature, and stirred for 1 h. The reaction mixture was cooled by an ice bath, quenched with water, and acidified to pH 4-5 by addition of concentrated HCl. The solvent was removed under reduced pressure. The residue was dissolved in methylene chloride, washed with water (2 times), dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography to give the title compound as an oil (250 mg). LCMS m/z=213.1 [M−H2O+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447041B2
出典データセットuspto-grants-2016_09
ORD IDord-47fe68485ad74b8da690b0ca7fd0be1b
出典メモuspto-grants-2016_09