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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 61871Generated: October 25, 2026

Potassium Carbonate → 2-Methyl-2-(4-vinylphenyl)propanoic acid

https://huagongshe.com/reaction/61871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphineHCID 11776—
Reactant2-(4-Bromophenyl)-2-methylpropanoic acidHCID 10933679—
ReactantPotassium vinyltrifluoroborateHCID 23679353—
Catalystpalladium(II) acetateHCID 167845—
Solvent1-PropanolHCID 1031—
Product2-Methyl-2-(4-vinylphenyl)propanoic acidHCID 66834551598.4%

Reaction Steps

2-(4-Bromophenyl)-2-methylpropanoic acid (30 g), PPh3 (5.0 g), potassium vinyltrifluoroborate (24.8 g), potassium carbonate (51.2 g), and palladium acetate (1.43 g) were dissolved in 1-propanol (198 ml) and distilled water (99 ml). After deaeration, the mixture was stirred under reflux for 6 hrs under nitrogen atmosphere. Insoluble matters were removed by filtration and washed with 1-propanol (210 ml). The filtrate was then concentrated under reduced pressure. Concentrated residues were partitioned between CPME (300 ml) and distilled water (150 ml, comprising 4.17 ml of ethylenediamine) The organic layer was removed and the aqueous layer was adjusted to pH 5 by using 2 N hydrochloric acid. The aqueous layer was extracted with a mixture of isopropyl acetate (240 ml) and heptane (240 ml). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. Ethanol (300 ml) was added thereto for suspending and washing the resultant. The solid was removed by Celite filtration, and the filtrate was concentrated under reduced pressure to obtain the title compound (21.7 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440922B2
Source datasetuspto-grants-2016_09
ORD IDord-c54bf4c4ceb34b8ca33306f12197988e
Source noteuspto-grants-2016_09