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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836423Generated: October 26, 2026

4-Fluorophenylboronic acid → Methyl 4-methoxy-2-(4-fluorophenyl)benzoate

https://huagongshe.com/reaction/1836423

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorophenylboronic acidHCID 285645—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 4-methoxy-2-trifluoromethanesulphonylbenzoateHCID 23499549—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductMethyl 4-methoxy-2-(4-fluorophenyl)benzoateHCID 23499548131%

Reaction Steps

Saturated aqueous sodium hydrogen carbonate solution (50 ml) was added to a solution of methyl 4-methoxy-2-trifluoromethanesulphonylbenzoate (6.3 g.) and 4-fluorobenzeneboronic acid (3.36 g.) in DME (150 ml) at ambient temperature under an argon atmosphere. Tetrakis(triphenylphosphine) palladium (928 mg.) was added and the reaction heated and stirred at reflux for 3.5 hours resulting in a homogeneous solution. After cooling to ambient temperature, the reaction was partitioned between ethyl acetate and water. The organic phase was washed with 2N hydrochloric acid, water and brine, filtered through 1PS filter paper and the solvent removed to give methyl 4-methoxy-2-(4-fluorophenyl)benzoate as a yellow-oily solid (7.2 g) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777438B2
Source datasetuspto-grants-2004_08
ORD IDord-13bb38d1e4df4201a20264da3bfffdc2
Source noteuspto-grants-2004_08