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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929249Generated: October 30, 2026

Potassium Carbonate → 4'-Bromo-4-ethoxy-2,3-difluoro-1,1'-biphenyl

https://huagongshe.com/reaction/1929249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-4-iodobenzeneHCID 11522—
ReactantB-(4-Ethoxy-2,3-difluorophenyl)boronic acidHCID 15135235—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4'-Bromo-4-ethoxy-2,3-difluoro-1,1'-biphenylHCID 1206745194%

Reaction Conditions

Temperature25 °C

Reaction Steps

4-Bromoiodobenzene (1) (20.0 g), 4-ethoxy-2,3-difluorophenylboronic acid (2) (14.4 g), potassium carbonate (29.3 g), Pd(Ph3P)2Cl2 (1.49 g), toluene (100 ml), Solmix A-11 (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, and an extractive operation to an organic phase was carried out. The organic phase obtained was fractionated, washed with water, and then dried over anhydrous magnesium sulfate. The solution obtained was concentrated under reduced pressure, and the residue obtained was purified with a fractional operation by means of column chromatography using toluene as the eluent and silica gel as the stationary phase powder. The product was further purified by means of recrystallization from Solmix A-11 and dried, giving 20.8 g of 4-ethoxy-4′-bromo-2,3-difluoro-1,1′-biphenyl (3). The yield based on the compound (1) was 94.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08187494B2
Source datasetuspto-grants-2012_05
ORD IDord-f6f6c893b69d422b9dd7dda165051522
Source noteuspto-grants-2012_05