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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540757Generated: October 29, 2026

Potassium Carbonate → 3-[1-ethyl-5-(4-fluoro-2-nitrophenoxy)-1H-pyrazol-3-yl]benzonitrile

https://huagongshe.com/reaction/540757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,5-DifluoronitrobenzeneHCID 67767—
Reactant3-(1-ethyl-5-oxo-2,5-dihydro-1H-pyrazol-3-yl)benzonitrileHCID 67111059—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product3-[1-ethyl-5-(4-fluoro-2-nitrophenoxy)-1H-pyrazol-3-yl]benzonitrileHCID 67111584—

Reaction Conditions

Temperature80 °C

Reaction Steps

1,4-difluoro-2-nitrobenzene (2.06 g, 9.85 mmol, 3 equiv) was added to a stirring mixture of 3-(1-ethyl-5-oxo-2,5-dihydro-1H-pyrazol-3-yl)benzonitrile (0.70 g, 3.28 mmol, 1 equiv) and potassium carbonate (1.36 g, 9.85 mmol, 3 equiv) in DMSO (6.57 mL). The reaction mixture was stirred at 80° C. for 20 minutes then cooled to 22° C. and diluted with water. The mixture was extracted with ethyl acetate, and then the organic layer was washed sequentially with water (two times) and saturated aqueous sodium chloride. The washed solution was dried over anhydrous magnesium sulfate. The drying agent was filtered, and the filtrate was concentrated in vacuo to give the 3-[1-ethyl-5-(4-fluoro-2-nitrophenoxy)-1H-pyrazol-3-yl]benzonitrile. The crude reaction product was taken into the next step without further purification. Calcd (M+1)+: 353.1. Found: 353.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871796B2
Source datasetuspto-grants-2014_10
ORD IDord-7cd8692b71a2491a9793de275956561a
Source noteuspto-grants-2014_10