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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1071781Erstellt: 27. Oktober 2026

Pyridine → N-{4[(acetyloxy)imino]-2,5-cyclohexadien-1-ylidene}aniline

https://huagongshe.com/reaction/1071781

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktTolueneHCID 1140—
EduktAcetic AnhydrideHCID 7918—
Edukt4-NitrosodiphenylamineHCID 9074—
LösungsmittelWaterHCID 962—
ProduktN-{4[(acetyloxy)imino]-2,5-cyclohexadien-1-ylidene}anilineHCID 20801492—

Reaktionsbedingungen

Temperatur5 °C

Reaktionsschritte

A solution was prepared by mixing 4-nitrosodiphenylamine, 19.8 grams, (0.10 mole), pyridine, 8.6 grams, (0.11 mole), and toluene, 10 mL, in a suitable reaction flask. The solution was cooled to 5° C. and acetic anhydride, 11.22 grams, (0.11 mole) was added slowly. The mixture was stirred for 2 hours and allowed to come to room temperature. The reaction mixture was mixed with a quantity of water, allowed to stand until the water layer separated, and the water layer was discarded. The toluene solution was evaporated to leave 21.4 grams of a solid residue, 96% of theory. The material melted at 63-65° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06906121B2
Quelldatensatzuspto-grants-2005_06
ORD IDord-ec5e0582668946a39c1d9a9f080e78be
Quellennotizuspto-grants-2005_06