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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167652Generated: October 25, 2026

Ethyl isonicotinate → 2-Cyano-2-[4-(1,1-dimethylethyl)phenyl]-1-(4-pyridyl)ethanone

https://huagongshe.com/reaction/1167652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isonicotinateHCID 15291—
Reactant(4-tert-Butylphenyl)acetonitrileHCID 76784—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Product2-Cyano-2-[4-(1,1-dimethylethyl)phenyl]-1-(4-pyridyl)ethanoneHCID 2299374435%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of ethyl isonicotinate (12 g) and 4-(1,1-Dimethylethyl)phenylacetonitrile (9.1 g) in tert-butyl alcohol (36 mL), was added potassium tert-butoxide (7.3 g), and the mixture was stirred at 100° C. for 3 h. After cooling, the resulting mixture was dissolved in water and washed with isopropyl ether. The aqueous phase was adjusted to pH 7.0 with 2 N hydrochloric acid and extracted with ethyl acetate. The extract was washed with water, dried, and the solvent was evaporated. The crystalline residue was recrystallized from ethyl acetate-isopropyl ether to obtain 2-cyano-2-[4-(1,1-dimethylethyl)phenyl]-1-(4-pyridyl)ethanone (5.09 g, yield 35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620825B1
Source datasetuspto-grants-2003_09
ORD IDord-c388df1a2ee94b51a832892f3e659873
Source noteuspto-grants-2003_09