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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712196Generated: November 1, 2026

Potassium Carbonate → HCID 68616940, compound

https://huagongshe.com/reaction/1712196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphineHCID 11776—
Reactant4-Fluoro-phenylboric acidHCID 21939771—
ReactantHCID 68615191HCID 68615191—
CatalystTetrabutylammonium BromideHCID 74236—
CatalystHCID 178418476HCID 178418476—
SolventEthanol toluene waterHCID 86587398—
ProductHCID 68616940HCID 68616940—

Reaction Steps

A mixture of 7.00 g (=18.61 mmol) of the above 2-[2-(3-fluoro-4-iodophenyl)ethyl]naphthalene, 3.12 g (=22.30 mmol) of 4-fluorophenylboric acid, 3.86 g (=27.93 mmol) of K2CO3, 1.50 g (=4.65 mmol) of tetrabutylammonium bromide, 0.39 g (=0.56 mmol) of dichlorobis(triphenylphosphine)palladium(II), 0.30 g (1.12 mmol) of triphenylphosphine and 60 ml of a mixed solvent of toluene/water/ethanol in a ratio of 1:1:1 was stirred for 4 hours with reflux. The reaction mixture obtained was extracted thrice with toluene, and then the extract was washed thrice with water and dried with anhydrous MgSO4. After the solvent was evaporated under a reduced pressure, the obtained orange solid of 8.48 g was purified with silica gel chromatography using heptane/toluene in a ratio of 5:1 as the eluent to obtain a white solid of 7.37 g, which was further recrystallized using a mixed solvent of Solumix/heptane in a ratio of 1:1 to obtain the target compound in an amount of 5.02 g. The product was characterized as the target compound based on results of various instrumental analyses, and the phase transition of the product is notated as “C 108.1 I”.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790915B2
Source datasetuspto-grants-2010_09
ORD IDord-a70c005585534082a5b23b7877cddb72
Source noteuspto-grants-2010_09