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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304494Generated: November 1, 2026

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

https://huagongshe.com/reaction/2304494

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 then treated at room temperature under nitrogen with sodium borohydride in a portion wise manner. After addition, the reaction mixture was stirred for 4 hours, treated with a saturated solution of aqueous ammonium sulfate (50 mL) and ethyl acetate (100 mL). The organic layer was separated, dried (MgSO4), and evaporated in vacuo. The residue was purified on a silica gel 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 numberUS06436929B1
Source datasetuspto-grants-2002_08
ORD IDord-b1fbfd5e62eb46bf957bf7519b97423c
Source noteuspto-grants-2002_08