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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773063Generated: November 1, 2026

Potassium Carbonate → HCID 89568606, compound

https://huagongshe.com/reaction/1773063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantHCID 71039292HCID 71039292—
ReactantHCID 89568605HCID 89568605—
Catalystpalladium(II) acetateHCID 167845—
Solvent1-ButanolHCID 263—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 89568606HCID 89568606—

Reaction Conditions

Temperature95 °C

Reaction Steps

In a stream of argon, 517 mg (0.996 mmol) of 2-[5-(anthracen-9-yl)-3-chlorophenyl]-4,6-diphenylpyrimidine, 299 mg (1.20 mmol) of 4-(quinolin-2-yl)phenylboronic acid and 4.5 mg (20 μmol) of palladium acetate and 29.6 mg (60 μmol) of 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl were suspended in a toluene (4.5 mL)/n-butanol (0.5 mL) mixed solvent, and the suspension was heated to 95° C. 800 μL (2.40 mmol) of an aqueous 3.0M potassium carbonate solution was gradually dropwise added to the mixture, and the mixture was stirred at that temperature for 2 hours. Then the reaction mixture was left to be cooled to room temperature, and water was added to the reaction mixture. Then the deposited solid was collected by filtration to give 645 mg of target 2-[5-(anthracen-9-yl)-4′-(quinoline-2-yl) biphenyl-3-yl]-4,6-diphenylpyrimidine as a white solid (yield, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09252368B2
Source datasetuspto-grants-2016_02
ORD IDord-4874cf75710c4b4baa5d767d06eba6e6
Source noteuspto-grants-2016_02