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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1085588Erstellt: 26. Oktober 2026

Sodium Chloride → 4-[2-[2,3-Dihydro-2-(4-fluorophenyl)-2-methyl-3-oxo-5-furanyl]ethenyl]benzonitrile

https://huagongshe.com/reaction/1085588

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ChlorideHCID 5234—
EduktSodium HydroxideHCID 14798—
Edukt4-CyanobenzaldehydeHCID 66042—
Edukt2-(4-Fluorophenyl)-2,5-dimethylfuran-3(2H)-oneHCID 15086704—
LösungsmittelEthanolHCID 702—
Produkt4-[2-[2,3-Dihydro-2-(4-fluorophenyl)-2-methyl-3-oxo-5-furanyl]ethenyl]benzonitrileHCID 5364862638,7%

Reaktionsschritte

To a solution of p-cyanobenzaldehyde (1.6 g, 11.8 mM) and 2,5-dimethyl-2-(4-fluorophenyl)-3(2H)-furanone (2.0 g, 9.8 mM) in ethanol (75 mL), was added 1N aqueous sodium hydroxide (1.0 mL, 1 mM). After the reaction solution was stirred at room temperature for two days, saturated aqueous sodium chloride (400 mL) was added. The aqueous layer was extracted with dichloromethane (3×100 mL). The combined dichloromethane extracts were washed with saturated aqueous sodium chloride (50 mL), dried over MgSO4, filtered and concentrated to give an orange liquid. The crude product was purified by chromatography (silica gel, pet. ether-ethyl acetate) to give a yellow crystalline solid (1.2 g, 38% yield), m.p. 140°-142° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05010102
Quelldatensatzuspto-grants-1991_04
ORD IDord-1692325ce1324ce384727a815659feab
Quellennotizuspto-grants-1991_04