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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260902Generated: October 29, 2026

Potassium Carbonate → 3-Fluoro-4'-propylbiphenyl

https://huagongshe.com/reaction/2260902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-3-fluorobenzeneHCID 14082—
Reactant(4-Propylphenyl)boronic acidHCID 4100861—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product3-Fluoro-4'-propylbiphenylHCID 1852110880.6%

Reaction Conditions

Temperature25 °C

Reaction Steps

Into a reaction vessel under an atmosphere of nitrogen, 4-propyl phenylboronic acid (T16; 200.0 g), 1-bromo-3-fluorobenzene (T8; 177.8 g), potassium carbonate (281.9 g), Pd(Ph3P)2Cl2 (7.2 g), toluene (600 ml), and Solmix A-11 (600 ml) were put and heated under reflux for 2 hours. After the reaction mixture had been cooled to 25° C., the solution was poured into water (2,000 ml) and toluene (1,000 ml), and mixed. The mixture was then allowed to stand to be separated into two layers of an organic layer and an aqueous layer. Extraction into an organic layer was carried out and the resulting organic layer was fractionated. The extracts were washed with water, and dried over anhydrous magnesium sulfate. The resulting solution was concentrated under reduced pressure, and the residue was purified by means of fraction-collecting column chromatography using heptane as the eluent and silica gel as the stationary phase powder. The solution was further purified by recrystallization from Solmix A-11 and then dried, whereby 175.5 g of 3-fluoro-4′-propylbiphenyl (T17) was obtained. The yield based on the compound (T8) was 80.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846514B2
Source datasetuspto-grants-2010_12
ORD IDord-748b112e6ada4a7e9ddd25cdd65008f6
Source noteuspto-grants-2010_12