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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095853Generated: October 31, 2026

Dabco → 1-(4-Fluorophenyl)-2-oxo-6-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrile

https://huagongshe.com/reaction/2095853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDabcoHCID 9237—
Reactant2-Cyano-N-(4-fluorophenyl)acetamideHCID 693148—
Reactant(3E)-4-Ethoxy-1,1,1-trifluoro-3-buten-2-oneHCID 5709222—
SolventHydrochloric AcidHCID 313—
Solvent2-MethoxyethanolHCID 8019—
SolventEthyl AcetateHCID 8857—
Product1-(4-Fluorophenyl)-2-oxo-6-(trifluoromethyl)-1,2-dihydropyridine-3-carbonitrileHCID 581584837.3%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 2-cyano-N-(4-fluorophenyl)acetamide (2 g, 11.2 mmol) and (3E)-4-ethoxy-1,1,1-trifluorobut-3-en-2-one (2.26 g, 13.4 mmol) in dimethyleneglycol monomethylether (20 mL) was added 1,4-diazabicyclo[2.2.2]octane (1.26 g, 11.2 mmol), and the mixture was stirred at 120° C. for 6 hr. The reaction mixture was diluted with 1N hydrochloric acid and ethyl acetate, and the mixture was extracted 3 times with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and filtered. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (NH silica gel, ethyl acetate/hexane=1/2→1/1) to give a white solid. The white solid was washed with ethyl acetate and collected by filtration to give the title compound (230 mg, 7.2%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445509B2
Source datasetuspto-grants-2013_05
ORD IDord-479ff93a4f734902bc4102c156dd5156
Source noteuspto-grants-2013_05