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HRID 458121作成日:2026年10月25日

Acetone → 2-(5-Fluoro-2-methoxyphenyl)propan-2-ol

https://huagongshe.com/reaction/458121

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物2-Bromo-4-fluoroanisoleHCID 136292—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物2-(5-Fluoro-2-methoxyphenyl)propan-2-olHCID 2228488885%

反応条件

温度-78 °C

反応手順

To a stirred solution of 2-bromo-4-fluoro anisole (4.1 g, 20 mmol) in anhydrous THF (40 mL) cooled to −78° C. and maintained under an atmosphere of argon was added n-butyl lithium (8.8 mL of 2.5 M solution in hexanes, 22 mmol). After stirring at −78° C. for 45 minutes, the reaction mixture was treated with anhydrous acetone (5 mL). After 15 minutes, the reaction mixture was quenched with a saturated solution of ammonium chloride and extracted with three 50 mL portions of methylene chloride. Combined extracts were washed with three 25 mL portions of water, dried over anhydrous sodium sulfate, and the solvent was evaporated to give 2-(5-fluoro-2-methoxyphenyl)propan-2-ol as a light brown thick oil (85% yield) which solidified on standing. The crude product was used for the next reaction without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07189758B2
出典データセットuspto-grants-2007_03
ORD IDord-f5210dcb51a346028c940970d24e133b
出典メモuspto-grants-2007_03