Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 21699Erstellt: 23. Oktober 2026

Potassium Hydroxide → 2-(4-Methoxybenzylamino)-4,6-dimethylnicotinamide

https://huagongshe.com/de/reaction/21699

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium HydroxideHCID 14797—
EduktAcetylacetoneHCID 31261—
Edukt4-MethoxybenzylamineHCID 75452—
EduktEthyl 2-(4-methoxybenzylamino)-4,6-dimethylnicotinateHCID 19933377—
EduktEthyl beta-amino-beta-ethoxyacrylate hydrochlorideHCID 53395434—
LösungsmittelEthanolHCID 702—
Produkt2-(4-Methoxybenzylamino)-4,6-dimethylnicotinamideHCID 1993337670%

Reaktionsbedingungen

Temperatur22 °C

Reaktionsschritte

In a three-necked flask containing ethanol (6.12mL) is added ethyl 3-amino-3-ethoxyacrylate hydrochloride(3g, 15.3mmol). The solution is treated with 4-methoxybenzylamine(2mL, 15.3mmol) and the mixture is stirred at 22° C. for 1.5 h. The reaction mixture was heated to 80° C. for 3 h. The reaction is cooled to 22° C. and an ethanolic solution of potassium hydroxide (0.86 g, 15.3 mmol, 25.0 mL of ethanol) is added. Neat 2,4-pentanedione (1.57 mL, 15.3 mmol) is added to the solution dropwise over 15 minutes at room temperature. The reaction mixture is aged at room temperature for 24 hours. During the age the nicotinate precipitates out of the reaction as does KCl. The reaction mixture is concentrated in vacuo. The crude mixture is chromatographed on silica gel to afford a 70% yield of the product, ethyl 2-(4-methoxybenzylamino )-4,6-dimethylnicotinate, 27.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05424432
Quelldatensatzuspto-grants-1995_06
ORD IDord-df276dfc5b8f41f39fbda1b70b2c26ca
Quellennotizuspto-grants-1995_06