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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2079176Erstellt: 26. Oktober 2026

Veratraldehyde → (3,4-Dimethoxyphenyl)-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylamino]acetonitrile

https://huagongshe.com/reaction/2079176

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktVeratraldehydeHCID 8419—
EduktTrimethylsilyl cyanideHCID 82115—
EduktYtterbium triflateHCID 2733225—
Edukt4-(5-Methyl-1,2,4-oxadiazol-3-yl)anilineHCID 18188176—
Edukt2-{3-[(4-carbamimidoylphenylamino)-(2-fluoro-4,5-dimethoxyphenyl)methyl]5-oxo-4,5-dihydro-[1,2,4]triazol-1-yl}benzoic Acid TrifluoroacetateHCID 136337083—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(3,4-Dimethoxyphenyl)-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylamino]acetonitrileHCID 59517365—

Reaktionsschritte

After adding 0.887 g of 4-(5-methyl-[1,2,4]oxadiazol-3-yl)phenylamine, 0.831 g of 3,4-dimethoxybenzaldehyde, 1g of MS3A and 1 ml of trimethylsilyl cyanide to a solution of 0.31 g of Yb(OTf)3 in 20 ml of dichloromethane under a nitrogen atmosphere, the mixture was stirred at room temperature for 22 hours. After then adding 200 ml of ethyl acetate to the reaction mixture, it was filtered through celite and the celite was washed with 200 ml of ethyl acetate. The organic layers were combined and washed with water and saturated brine, and then dried over anhydrous magnesium sulfate. The desiccating agent was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane) to give the title compound (1.75 g) as a light yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07928228B2
Quelldatensatzuspto-grants-2011_04
ORD IDord-fc1e68c7439e467da9179750f8e9e856
Quellennotizuspto-grants-2011_04