Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179095Generated: November 1, 2026

Potassium Carbonate → (3-Phenylphenyl)boronic acid

https://huagongshe.com/reaction/1179095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphineHCID 11776—
ReactantPhenylboronic AcidHCID 66827—
Reactant(3-Bromophenyl)boronic acidHCID 2734318—
Catalystpalladium(II) acetateHCID 167845—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(3-Phenylphenyl)boronic acidHCID 273431587%

Reaction Steps

Phenyl boronic acid (1) (106.2 g, 871.4 mmol), 3-bromophenylboronic acid (2) (35.0 g, 174.2 mmol), palladium acetate (9.8 g, 4.357 mmol), triphenylphosphine (4.64 g, 17.4 mmol), and 2M K2CO3 aqueous solution (470 ml) were added to 950 mL of dimethoxyethane and refluxed for 17 hours. The mixture was cooled to room temperature and the aqueous layer was separated from the organic layer. The aqueous layer was then extracted twice with 200 mL of ethyl acetate. The organic layers were combined and washed with brine and dried over magnesium sulfate. The solids were removed by vacuum filtration and the organic solvent evaporated to the crude product. The crude product was purified by Kugelehor distillation to give of 3 (30 g, 86.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279232B2
Source datasetuspto-grants-2007_10
ORD IDord-1ee2d78665db4b76a635dd67baf81b7c
Source noteuspto-grants-2007_10