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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1611721Erstellt: 23. Oktober 2026

Cyclohexanone → Cyclohexene-1-yl acetate

https://huagongshe.com/de/reaction/1611721

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclohexanoneHCID 7967—
Edukt2-NitrocyclohexanoneHCID 521241—
ProduktCyclohexene-1-yl acetateHCID 74019—

Reaktionsschritte

nitrocyclohexanone process in which cyclohexanone is acetylated to obtain cyclohexenyl acetate, the obtained cyclohexenyl acetate is nitrated to obtain 2-nitrocyclohexanone, the obtained 2-nitrocyclohexanone is subjected to hydrolysis, thereby causing ring cleavage of the 2-nitrocyclohexanone to obtain nitrocapronic acid, the obtained nitrocapronic acid is hydrogenated to obtain ε-aminocapronic acid, and the obtained ε-aminocapronic acid is converted into ε-caprolactam.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06989444B2
Quelldatensatzuspto-grants-2006_01
ORD IDord-ffbdc2a802f54936a47ccf1690561474
Quellennotizuspto-grants-2006_01