Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886715Generated: November 3, 2026

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

https://huagongshe.com/reaction/1886715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4-iodobenzoateHCID 142891—
ReactantB-(4-Ethoxy-2,3-difluorophenyl)boronic acidHCID 15135235—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductEthyl 4-ethoxy-2,3-difluoro-4'-biphenylbenzoateHCID 66682456108.6%

Reaction Conditions

Temperature25 °C

Reaction Steps

Ethyl 4-iodobenzoate (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 added to a reaction vessel under an atmosphere of nitrogen, and heated to reflux for 2 hours. After the reaction solution had been cooled to 25° C., it was poured into water (500 ml) and toluene (500 ml), and mixed with them. The mixture was then allowed to stand until it had separated into two phases of organic and aqueous phases, and the extraction into an organic phase was carried out. The resulting organic phase was separated, and washed with water, and then dried over anhydrous magnesium sulfate. The solution was concentrated under reduced pressure, and the resulting residue was purified by column chromatography using silica gel as a stationary phase powder and toluene as an eluent. The product was further purified by recrystallization from ethanol and dried to give ethyl 4-ethoxy-2,3-difluoro-4′-biphenylbenzoate (3) (18.8 g). The yield based on the compound (1) was 67.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501038B2
Source datasetuspto-grants-2013_08
ORD IDord-abd297a21b9d4e0aa6363476838f09de
Source noteuspto-grants-2013_08