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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595256Generated: November 3, 2026

Water → Ethyl 4'-methoxy[1,1'-biphenyl]-4-carboxylate

https://huagongshe.com/reaction/1595256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl 4-bromobenzoateHCID 22043—
ReactantCesium fluorideHCID 25953—
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductEthyl 4'-methoxy[1,1'-biphenyl]-4-carboxylateHCID 2764348—

Reaction Conditions

Temperature85 °C

Reaction Steps

A stirred mixture of 4-bromobenzoic acid, ethyl ester (23.6 g, 103 mmol), 4-methoxyphenylboronic acid (15.6 g, 103 mmol), tetrakis(triphenylphosphine)palladium (0) (2.0 g, 1.73 mmol) and powdered caesium fluoride (30.0 g, 200 mmol) in 1,2-dimethoxyethane (300 mL) is heated at 85° C. for 3 h. The mixture is then treated with water (500 mL) and extracted with ethyl acetate (3×100 mL). The combined extracts are washed (saturated NaCl), dried (Na2SO4), filtered and the solvent is evaporated off under reduced pressure to yield the crude product which is purified by chromatography (silica gel, 5% ethyl acetate/95% cyclohexane) to 4′-methoxy-[1,1′-biphenyl]-4-carboxylic acid, ethyl ester as a colourless crystalline solid, m.p. 103-104° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288092B1
Source datasetuspto-grants-2001_09
ORD IDord-bbc97165d7ac4f128a035f4c588a0810
Source noteuspto-grants-2001_09