Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241291Generated: October 25, 2026

Potassium Carbonate → 2,5-Difluoro-4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]nitrobenzene

https://huagongshe.com/reaction/1241291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,2,4-Trifluoro-5-nitrobenzeneHCID 75012—
Reactant1-Methyl-6-trifluoromethylpyrimidine-2,4-dioneHCID 11435480—
SolventDimethyl SulfoxideHCID 679—
Product2,5-Difluoro-4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]nitrobenzeneHCID 1211550943%

Reaction Conditions

Temperature80 °C

Reaction Steps

First, 1.77 g of 2,4,5-trifluoronitrobenzene and 1.94 g of 3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidine were dissolved in 10 ml of dimethylsulfoxide, to which 1.52 g of anhydrous potassium carbonate was added at room temperature, and the mixture was stirred at 80° C. for 1 hour. The reaction mixture was cooled to room temperature and then poured into ice water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated. The residue was subjected to silica gel column chromatography to give 1.51 g of 2,5-difluoro-4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2, 3,6-tetrahydropyrimidin-1-yl]nitrobenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115544B2
Source datasetuspto-grants-2006_10
ORD IDord-264039e5b66b4cc2bb69940ffb6d9a1c
Source noteuspto-grants-2006_10