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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1294167Erstellt: 27. Oktober 2026

Dimethylformamide → 2-[3-Methoxy-4-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]nicotinonitrile

https://huagongshe.com/reaction/1294167

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktSodium hydrideHCID 24758—
Edukt2-ChloronicotinonitrileHCID 81079—
Edukt3-Methoxy-4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyl alcoholHCID 57315820—
LösungsmittelWaterHCID 962—
Produkt2-[3-Methoxy-4-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]nicotinonitrileHCID 6888355290%

Reaktionsschritte

To a mixture of 3-methoxy-4-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyl alcohol (4.00 g), 2-chloro-3-cyanopyridine (1.62 g) and N,N-dimethylformamide (40 mL) was added sodium hydride (60%, oil, 515 mg) under ice-cooling. The reaction mixture was stirred at room temperature for 15 hrs. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated. The obtained crystals were recrystallized from ethyl acetate-hexane to give 2-[3-methoxy-4-[(5-methyl-2-phenyl-4-oxazolyl)methoxy]benzyloxy]nicotinonitrile as pale-yellow crystals (4.50 g, 90%). melting point: 117-118° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07238716B2
Quelldatensatzuspto-grants-2007_07
ORD IDord-513794fbd23a49d89dfbb88630aae61b
Quellennotizuspto-grants-2007_07