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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259295Generated: November 3, 2026

1-(3-Bromo-4-fluorophenyl)ethan-1-one → 1-(3-Bromo-4-fluorophenyl)ethanol

https://huagongshe.com/reaction/1259295

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Bromo-4-fluorophenyl)ethan-1-oneHCID 70508—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
Product1-(3-Bromo-4-fluorophenyl)ethanolHCID 20785306—

Reaction Steps

A solution of 1-(3-bromo-4-fluorophenyl)ethanone (15.0 g, 69 mmol) in tetrahydrofuran (200 mL) was treated with sodium borohydride (5.3 g, 138 mmol) at 0° C. After the addition, the ice bath was removed, and the mixture was stirred at room temperature for 30 minutes and at reflux overnight. After cooling, 1N HCl (10 mL) was slowly added and the reaction mixture was concentrated. The residue was partitioned between ethyl acetate and brine. The organic phase was washed with water, and concentrated. The residue was purified by flash chromatography (30% ethyl acetate in hexane) to provide the title compound. MS (DCI/NH3) m/z 220 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466150B2
Source datasetuspto-grants-2013_06
ORD IDord-17f818d0fe3f4d93a8a48433303b2303
Source noteuspto-grants-2013_06