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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385644Generated: November 1, 2026

Potassium Carbonate → 1-(4-Chlorophenyl)-1-(2-fluoro-3-(4-fluoro-3-phenoxyphenyl)prop-1-enyl)cyclopropane

https://huagongshe.com/reaction/1385644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(4-Fluoro-3-phenoxyphenyl)-boronic acidHCID 21185404—
Reactant1-(p-Chlorophenyl)-1-(3-bromo-2-fluoropropenyl)cyclopropaneHCID 53765764—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product1-(4-Chlorophenyl)-1-(2-fluoro-3-(4-fluoro-3-phenoxyphenyl)prop-1-enyl)cyclopropaneHCID 2118540563%

Reaction Steps

Under a nitrogen atmosphere, a mixture of 1-(p-chlorophenyl)-1-(3-bromo-2-fluoropropenyl)cyclopropane, (Z)—(0.434 g, 1.5 mmol), 4-fluoro-3-phenoxybenzene-boronic acid (0.452 g, 1.95 mmol), potassium carbonate (1.86 g, 13.5 mmol) and bis(dibenzylideneacetone)-palladium(O) (Pd(dba)2, 4.3 mg, 0.075 mmol) in toluene is heated at 80° C. for one hour, cooled to room temperature, diluted with water, and filtered through diatomaceous earth. The phases are separated and the aqueous phase is extracted with ethyl acetate. The organic phase and ethyl acetate extract are combined, washed with water, dried over anhydrous sodium sulfate and concentrated in vacuo to obtain a residue. Flash column chromatography of the residue using silica gel and a 3:20 methylene chloride/hexanes solution gives the title product as an oil (0.274 g, 63% yield) which is identified by NMR spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262319B1
Source datasetuspto-grants-2001_07
ORD IDord-dd21a8bbea0a45a8a1008262cd4bbe26
Source noteuspto-grants-2001_07