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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511477Generated: November 3, 2026

Potassium Carbonate → Ethyl 4-ethoxy-2,3-difluoro-4'-biphenylcarboxylate

https://huagongshe.com/reaction/1511477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantB-(4-Ethoxy-2,3-difluorophenyl)boronic acidHCID 15135235—
ReactantEthyl 4-iodoethylbenzoateHCID 66963157—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductEthyl 4-ethoxy-2,3-difluoro-4'-biphenylcarboxylateHCID 6696250574.7%

Reaction Conditions

Temperature25 °C

Reaction Steps

Ethyl 4-iodoethylbenzoate (1) (25.0 g), 4-ethoxy-2,3-difluorophenylboronic acid (2) (20.1 g), potassium carbonate (25.0 g), Pd/C (0.25 g), toluene (100 ml), ethanol (100 ml) and water (100 ml) were put in a reaction vessel under a nitrogen atmosphere, and heated under reflux for 2 hours. The reaction mixture was cooled to 25° C., and then poured into water (500 ml) and toluene (500 ml), and mixed. The mixture was then allowed to stand until it had separated into two phases of organic and aqueous phases. The extraction to an organic phase was carried out. The organic phase obtained was washed with water, and then dried over anhydrous magnesium sulfate. The solution obtained was concentrated under reduced pressure, and the residue obtained was purified by means of column chromatography (silica gel; toluene). The product was further purified by means of recrystallization from ethanol and dried, giving 18.8 g of ethyl 4-ethoxy-2,3-difluoro-4′-biphenylcarboxylate (3). The yield based on the compound (1) was 67.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08216489B2
Source datasetuspto-grants-2012_07
ORD IDord-2e055dfe50b24da982e00080b7d70ade
Source noteuspto-grants-2012_07