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HRID 30601作成日:2026年10月24日

Ammonium Chloride → (R)-2-fluoro-2-(3-bromophenyl)-1-ethanol

https://huagongshe.com/ja/reaction/30601

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物Sodium borohydrideHCID 4311764—
反応物(R)-2-fluoro-2-(3-bromophenyl)acetaldehydeHCID 86611665—
溶媒EthanolHCID 702—
溶媒DichloromethaneHCID 6344—
生成物(R)-2-fluoro-2-(3-bromophenyl)-1-ethanolHCID 68649207—

反応条件

温度0 °C

反応手順

A solution of (R)-2-fluoro-2-(3-bromophenyl)acetaldehyde in CH2Cl2 and ethanol is treated with NaBH4 (189 mg, 5 mmol), stirred for 30 min, cooled to 0° C., treated with saturated NH4Cl, warmed to room temperature, stirred vigorously for 1 h at room temperature and diluted with CH2Cl2. The phases are separated. The aqueous phase is extracted with CH2Cl2. The organic phase and the extracts are combined, washed with NaHCO3 and brine, dried over MgSO4 and concentrated in vacuo. The resultant residue is purified by column chromatography (5% EtOAc and hexane as eluant)to give (R)-2-fluro-2-(3-bromophenyl)-1-ethanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423158B2
出典データセットuspto-grants-2008_09
ORD IDord-9250e28ef0964ab3b68b4b1dfcef66c5
出典メモuspto-grants-2008_09