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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2304604Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/2304604

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl isonicotinateHCID 15291—
Edukt(4-tert-Butylphenyl)acetonitrileHCID 76784—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelWaterHCID 962—
Lösungsmitteltert-ButanolHCID 6386—
Produkt2-Cyano-2-[4-(1,1-dimethylethyl)phenyl]-1-(4-pyridyl)ethanoneHCID 2299374435%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06436966B1
Quelldatensatzuspto-grants-2002_08
ORD IDord-603c61fb75154f07ba90e9b15f3dfddd
Quellennotizuspto-grants-2002_08