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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1655250Erstellt: 26. Oktober 2026

Ethanol → N-(4-cyanophenyl)-4-amino-3-nitropyridine

https://huagongshe.com/reaction/1655250

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
Edukt4-AminobenzonitrileHCID 13396—
Edukt4-Chloro-3-nitropyridineHCID 2735781—
ProduktN-(4-cyanophenyl)-4-amino-3-nitropyridineHCID 19791284—

Reaktionsschritte

According to the method of J. C. S. Perkin Trans. I, 1979, 135, P-cyanoaniline (6.894 g, 58.4 mmol) was added to a solution of 4-chloro-3-nitropyridine (9.26 g, 58.4 mmol) in ethanol (200 ml) and the mixture was stirred at room temperature for 18 hours. The resulting yellow suspension was poured into 500 ml of ice-cold dilute ammonia and filtered. The solid was treated with 150 ml of boiling ethanol, cooled in ice, and filtered to give N-(4-cyanophenyl)-4-amino-3-nitropyridine, 12.15 g, as a bright yellow powder, m.p. 210°-211° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05250531
Quelldatensatzuspto-grants-1993_10
ORD IDord-9e795bb4c2e046ff92e974c5ef20aa72
Quellennotizuspto-grants-1993_10