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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191899Generated: November 2, 2026

Potassium Carbonate → 3-Chloro-biphenyl-4-carboxaldehyde

https://huagongshe.com/reaction/1191899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylboronic AcidHCID 66827—
Reactant4-Bromo-2-chlorobenzaldehydeHCID 14109109—
ReactantHeptane chloroformeHCID 21875152—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product3-Chloro-biphenyl-4-carboxaldehydeHCID 2144128466.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 5 g (22.78 mmol) of 4-bromo-2-chlorobenzaldehyde in 30 ml of tetrahydrofurane are successively added 3.47 g (28.47 mmol) of phenylboronic acid, 4.72 g (34.17 mmol) of potassium carbonate dissolved in 15 ml of water and 263 mg (0.01 equivalent) of tetrakis(triphenylphosphine) palladium. The reaction mixture is heated at 80° C. for 3 hrs. The reaction mixture is then cooled to ambient temperature and poured on 150 ml of brine. The watery layer is extracted three times with dichloromethane and the combined organic layers are successively washed by a 1M solution of sodium hydroxide, brine and filtered over a ChemElut cartridge to yield after concentration 4.6 g of a brown solid. Column chromatography (gradient heptane/chloroforme) yielded 3.29 g (65% yield) of 3-chlorobiphenyl-4-carbaldehyde as a white solid; mp=90-91° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680127B2
Source datasetuspto-grants-2014_03
ORD IDord-719752c716744dac81adc6439802d121
Source noteuspto-grants-2014_03