Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 27686Erstellt: 24. Oktober 2026

Ethyl cyanoacetate → Ethyl 5-amino-1-phenyl-1H-1,2,3-triazole-4-carboxylate

https://huagongshe.com/de/reaction/27686

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl cyanoacetateHCID 7764—
EduktAzidobenzeneHCID 69319—
EduktSodiumHCID 5360545—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
ProduktEthyl 5-amino-1-phenyl-1H-1,2,3-triazole-4-carboxylateHCID 253349—

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

A solution of sodium (2.04 g; 0.089 mole) in ethanol (50 ml) was added to a mixture of phenyl azide (11.9 g; 0.1 mole) and ethyl cyanoacetate (11.3 g; 0.1 mole) and the product gently warmed to 45° C. with stirring for 5 mins. After stirring at ambient temperature for a further 15 minutes the flask was immersed in water at room temperature for 3 hrs. A white solid separated which was filtered off after dilution of the mixture with water and washed with water. Recrystallisation from ethanol gave 18.4 g. (79%) of material of mp 124.5-125.5° C. (lit mp 126°; B. R. Brown, D. L. Hammick and S. G. Heritage J. Chem. Soc. 3820 [1953]).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04223032
Quelldatensatzuspto-grants-1980_09
ORD IDord-b3e067cf1f534ffe8363abbafa8f7d65
Quellennotizuspto-grants-1980_09