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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552026Generated: October 31, 2026

Potassium Carbonate → 3-Fluoro-4'-pentyl-1,1'-biphenyl

https://huagongshe.com/reaction/552026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Fluorophenylboronic acidHCID 2733986—
Reactant1-Bromo-4-pentylbenzeneHCID 2735599—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product3-Fluoro-4'-pentyl-1,1'-biphenylHCID 5932847684.7%

Reaction Conditions

Temperature25 °C

Reaction Steps

1-Bromo-4-pentylbenzene (T-1; 50.0 g), 3-fluorophenylboronic acid (31.4 g), potassium carbonate (91.2 g), Pd(Ph3P)2Cl2 (4.63 g), toluene (150 ml), Solmix A-11 (150 ml), and water (150 ml) were added to a reaction vessel under a nitrogen atmosphere, and heated under reflux for 3 hours. The reaction mixture was cooled to 25° C., and then poured into water (500 ml) and toluene (500 ml) and mixed. Then, the mixture was allowed to stand to be separated into two layers of organic and aqueous layers, and the extraction to an organic layer was carried out. The obtained organic layer was fractionated, washed with water, and then dried over anhydrous magnesium sulfate. The obtained solution was concentrated under reduced pressure, and the residue was purified with a fractional operation by means of column chromatography using heptane as the eluent and silica gel as the stationary phase powder. The product was further purified by recrystallization from Solmix A-11 and dried, whereby 45.2 g of 3-fluoro-4′-pentylbiphenyl (T-2) was obtained. The yield based on the compound (T-1) was 85%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951433B2
Source datasetuspto-grants-2011_05
ORD IDord-ef6c1de658d44edbbbd1391e97b77bc0
Source noteuspto-grants-2011_05