Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1526376Erstellt: 27. Oktober 2026

Potassium Iodide → 1-(Sec-butyl)-4-methoxy-2-oxo-1,2-dihydropyridine-3-carbonitrile

https://huagongshe.com/reaction/1526376

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
Edukt2-BromobutaneHCID 6554—
EduktCesium carbonateHCID 10796—
Edukt3-Pyridinecarbonitrile, 1,2-dihydro-4-methoxy-2-oxo-HCID 2786702—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
LösungsmittelSodium BicarbonateHCID 516892—
Produkt1-(Sec-butyl)-4-methoxy-2-oxo-1,2-dihydropyridine-3-carbonitrileHCID 11777003848%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a mixture of 4-methoxy-2-oxo-1,2-dihydropyridine-3-carbonitrile (500 mg), cesium carbonate (2.17 g), potassium iodide (553 mg) N,N-dimethylformamide (10 mL) and 1,2-dimethoxyethane (10 mL) was added 2-bromobutane (776 mg) at room temperature, and the mixture was stirred overnight at 60° C. The reaction mixture was diluted with saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted threetimes with ethyl acetate. The extracts were combined, washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (330 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09085578B2
Quelldatensatzuspto-grants-2015_07
ORD IDord-9d34407f90f241f1a9266b80a887fca7
Quellennotizuspto-grants-2015_07