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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384397Generated: October 30, 2026

Bromine → Ethyl 3′-bromo-4′-methoxy[1,1′-biphenyl]-4-carboxylate

https://huagongshe.com/reaction/1384397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantEthyl 4'-methoxy[1,1'-biphenyl]-4-carboxylateHCID 2764348—
SolventCarbon TetrachlorideHCID 5943—
ProductEthyl 3′-bromo-4′-methoxy[1,1′-biphenyl]-4-carboxylateHCID 85749597—

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of bromine (14.6 g, 91.3 mmol) in carbon tetrachloride (100 mL) is added to a stirred mixture of 4′-Methoxy-[1,1′-biphenyl]-4-carboxylic acid, ethyl ester (23.4 g, 91.3 mmol) and silica gal (100 g of particle size 0.040-0.063 mm: Merck 1.09385) in carbon tetrachloride (350 mL). The mixture is stirred at 20° C. for 4 h after which the silica gel is removed by filtration. The filtrate is washed with aqueous sodium hydrogen carbonate (200 mL of 1 M) followed by aqueous sodium thiosulphate (50 mL of 2 M), dried (Na2SO4), filtered and evaporated to dryness under reduced pressure to give the crude product which is recrystallised from ether-cyclohexane to give 3′-bromo-4′-methoxy-[1,1′-biphenyl]-4-carboxylic acid, ethyl ester as a colourless crystalline solid, m.p. 114-115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258843B1
Source datasetuspto-grants-2001_07
ORD IDord-3820fd2f66a848cbaaeb66fb3eadbf11
Source noteuspto-grants-2001_07