HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Cyclohexanone → Cyclohexene-1-yl acetate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Cyclohexanone | HCID 7967 | — |
| Edukt | 2-Nitrocyclohexanone | HCID 521241 | — |
| Produkt | Cyclohexene-1-yl acetate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06989444B2 |
| Quelldatensatz | uspto-grants-2006_01 |
| ORD ID | ord-ffbdc2a802f54936a47ccf1690561474 |
| Quellennotiz | uspto-grants-2006_01 |