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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 26088Erstellt: 25. Oktober 2026

4-Pyridinecarboxaldehyde → 4-(3-Methoxyphenyl)-1-(4-pyridyl)-1-pentene

https://huagongshe.com/reaction/26088

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-PyridinecarboxaldehydeHCID 13389—
EduktSodium hydrideHCID 24758—
Edukt3-(3-Methoxyphenyl)butyltriphenylphosphonium bromideHCID 20496878—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(3-Methoxyphenyl)-1-(4-pyridyl)-1-penteneHCID 54047177—

Reaktionsschritte

A mixture of 3-(3-methoxyphenyl)butyl triphenylphosphonium bromide (17.5 g., 35.4 mmoles) in dimethylsulfoxide (50 ml.) is added to 4-pyridinecarboxaldehyde (3.79 g., 35.4 mmoles) in tetrahydrofuran (40 ml.). The resulting mixture is then added dropwise to a slurry of 50% sodium hydride (1.87 g., 39 mmoles) in tetrahydrofuran (20 ml.) under a nitrogen atmosphere at 0°-5° C. Following completion of addition, the mixture is stirred for one hour at 0°-5° C. and then concentrated under reduced pressure. The concentrate is diluted with water (200 ml.) and then acidified with 6N HCl. The aqueous acid solution is extracted with benzene (4 × 50 ml.). It is then made basic and extracted with ethyl acetate (3 × 50 ml.). Evaporation of the combined extracts after drying (MgSO4) affords 4-(3-methoxyphenyl)-1-(4-pyridyl)-1-pentene as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04147872
Quelldatensatzuspto-grants-1979_04
ORD IDord-82dad07c0bb24612af1f92dd1c4e46fd
Quellennotizuspto-grants-1979_04