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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382170Generated: November 1, 2026

Ethyl Acetate → 3'-Ethoxy-3-fluorobiphenyl-4-amine

https://huagongshe.com/reaction/2382170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2-fluoroanilineHCID 123050—
Reactant3-Ethoxybenzeneboronic acidHCID 2773920—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
Product3'-Ethoxy-3-fluorobiphenyl-4-amineHCID 6699735595.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 4-bromo-2-fluoroaniline (3.2 g, 17.05 mmol), 2M K2CO3 (24 ml, 48.00 mmol), Pd(PPh3)4 (1.2 g, 1.02 mmol) in toluene (120 ml) under nitrogen atmosphere was added dropwise a solution of the 3-ethoxyphenylboronic acid (4.25 g, 25.61 mmol) in 31 ml of MeOH. The mixture was heated to 80° C. overnight and then cooled to room temperature. Ethyl acetate was added and washed twice with a K2CO3 aqueous solution. The organic layer was washed with brine, dried over magnesium sulphate, filtered and the solvent evaporated under vacuum. The residue obtained was purified by flash chromatography eluting with Hexane/AcOEt (from 10/1 to 8/1). The solid obtained was recrystallized in hexane to yield 3.78 g of the desired compound as a white solid. Yield=72%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258308B2
Source datasetuspto-grants-2012_09
ORD IDord-8a9e1fb6c9e7424885ef3a95956534e4
Source noteuspto-grants-2012_09