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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50734Generated: October 25, 2026

Ethyl Acetate → 1-(4-Amino-3'-fluoro[1,1'-biphenyl]-3-yl)ethanol

https://huagongshe.com/reaction/50734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium borohydrideHCID 4311764—
ReactantAmmonium SulfateHCID 6097028—
Reactant1-(4-Amino-3'-fluoro[1,1'-biphenyl]-3-yl)ethanoneHCID 22021891—
SolventMethanolHCID 887—
Product1-(4-Amino-3'-fluoro[1,1'-biphenyl]-3-yl)ethanolHCID 2202189967%

Reaction Steps

A solution of 1-(4-amino-3′-fluoro[1,1′-biphenyl]-3-yl)ethanone (3 g, 13 mmol) in anhydrous methanol (60 mL) was treated at rt under nitrogen with sodium borohydride in a portion wise manner. After addition, the reaction mixture was stirred for 4 hours, treated with a saturated aqueous ammonium sulfate solution (50 mL) and ethyl acetate (100 mL). The organic layer was separated, dried (MgSO4) and evaporated. The residue was purified on a silica gel column chromatography (hexane:ethyl acetate/3:1) to yield 1-(4-amino-3′-fluoro[1,1′-biphenyl]-3-yl)ethanol as a white solid (2 g, 67%): mp 136-137° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713478B2
Source datasetuspto-grants-2004_03
ORD IDord-f4797b5fcdf04f7aa4a77f4ea31c165e
Source noteuspto-grants-2004_03