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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552029Generated: October 31, 2026

Water → HCID 67172297, compound

https://huagongshe.com/reaction/552029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Fluorophenylboronic acidHCID 2733986—
CatalystPalladiumHCID 23938—
ProductHCID 67172297HCID 67172297—

Reaction Conditions

Temperature25 °C

Reaction Steps

The compound (T-31; 20.0 g), 3-fluorophenyl boronic acid (8.20 g), potassium carbonate (22.1 g), Pd/C (NX type; 0.114 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 5 hours. The reaction mixture was cooled to 25° C., and then poured into water (300 ml) and toluene (300 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 a mixed solvent of heptane/Solmix A-11 and dried, whereby 14.2 g of 2,3′-difluoro-4-(4-pentylcyclohexyl)-1,1′-biphenyl (T-32) was obtained. The yield based on the compound (T-31) was 78%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951433B2
Source datasetuspto-grants-2011_05
ORD IDord-ffb91d7f2abc4bf28b19574628554946
Source noteuspto-grants-2011_05