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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474937Generated: October 27, 2026

Potassium Carbonate → 4-(4-(Trifluoromethyl)phenyl)pyrimidin-2(1H)-one

https://huagongshe.com/reaction/474937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Chloro-2-methoxypyrimidineHCID 575230—
Reactant4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventHydrochloric AcidHCID 313—
SolventDimethyl SulfoxideHCID 679—
Product4-(4-(Trifluoromethyl)phenyl)pyrimidin-2(1H)-oneHCID 17851747322.2%

Reaction Conditions

Temperature95 °C

Reaction Steps

A suspension of 4-chloro-2-methoxypyrimidine (500 mg, 3.47 mmol), 4-(trifluoromethyl)phenylboronic acid (788 mg, 4.17 mmol), PdCl2(dppf) (283 mg, 0.347 mmol) and K2CO3 (958 mg, 6.94 mmol) in DMSO (10 mL) was degassed under reduced pressure for 45 min. The suspension was put under N2 and stirred at 95° C. for 20 h. The suspension was cooled, H2O was added and the suspension was filtered to afford a light colored solid. Flash chromatography on silica gel (hexanes/(1:1 EtOAc/hexanes), 100:0 to 0:100) afforded a white solid. The white solid was diluted with concentrated HCl solution (10 mL) and stirred at reflux for 4 h. The reaction was cooled, and the solution was neutralized with saturated NaHCO3 solution. The resulting suspension was filtered to afford 185 mg (22%) of the title compound as a white solid: ESI MS m/z 241 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637501B2
Source datasetuspto-grants-2014_01
ORD IDord-5b9fd642f48d4660821fe3e7aae7944a
Source noteuspto-grants-2014_01