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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 275893Erstellt: 25. Oktober 2026

3-Ethoxy-4-methoxybenzaldehyde → 3-(3-Ethoxy-4-methoxy-benzylamino)-propionic acid ethyl ester

https://huagongshe.com/reaction/275893

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Ethoxy-4-methoxybenzaldehydeHCID 244728—
Eduktbeta-Alanine, ethyl ester, hydrochlorideHCID 458475—
EduktSodium cyanoborohydrideHCID 5003444—
LösungsmittelEthanolHCID 702—
Produkt3-(3-Ethoxy-4-methoxy-benzylamino)-propionic acid ethyl esterHCID 5385854439,1%

Reaktionsschritte

A mixture of β-alanine ethyl ester hydrochloride (1.6 g), 3-ethoxy-4-methoxybenzaldehyde (1.8 g), sodium cyanoborohydride (0.42 g) and powdered 3Å molecular seives (2.5 g) in ethanol (25 ml) was stirred at ambient temperature for 24 hours. A further aliquot of sodium cyanoborohydride (0.42 g) was added and stirring was continued for a further 24 hours. The reaction mixture was filtered and the filtrate was evaporated. The residue was treated with ethyl acetate (100 ml) and the solution was washed with 10% aqueous potassium carbonate (50 ml), then twice with water (25 ml), then with brine (25 ml), then dried over magnesium sulphate and then evaporated. The residual oil was subjected to flash chromatography on silica eluting with a mixture of dichloromethane and methanol (95:5, v/v) to give the title compound as a colourless oil (1.1 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06352977B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-63a853df8ade4b968ea2376812013b75
Quellennotizuspto-grants-2002_03