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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30601Generated: October 26, 2026

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

https://huagongshe.com/reaction/30601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
Reactant(R)-2-fluoro-2-(3-bromophenyl)acetaldehydeHCID 86611665—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product(R)-2-fluoro-2-(3-bromophenyl)-1-ethanolHCID 68649207—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423158B2
Source datasetuspto-grants-2008_09
ORD IDord-9250e28ef0964ab3b68b4b1dfcef66c5
Source noteuspto-grants-2008_09