Hydrazine → Oxo-((2,2,6,6-tetramethylpiperidin-4-yl)amino)carbonylacetohydrazide
Reaktionsgleichung
[CH3:1][C:2]1([CH3:18])[CH2:7][CH:6]([NH:8][C:9](=[O:15])[C:10](OCC)=[O:11])[CH2:5][C:4]([CH3:17])([CH3:16])[NH:3]1.[NH2:19][NH2:20]>CO>[CH3:1][C:2]1([CH3:18])[CH2:7][CH:6]([NH:8][C:9]([C:10]([NH:19][NH2:20])=[O:11])=[O:15])[CH2:5][C:4]([CH3:17])([CH3:16])[NH:3]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
N-(2,2,6,6-tetramethyl-4-piperidinyl)-N'-aminooxamide was prepared by the hydrazinolysis of ethyl N-(2,2,6,6-tetramethyl-4-piperidinyl)oxamate with 64% aqueous hydrazine in methanol.
Quellen und Nachweise
- ORD-Eintrag
- ord-ca538c12b653412e87bf6d616423978c
- Quelldatensatz
- uspto-grants-1994_06
- Patentnummer
- US05318851
Notizen zur Reaktion
Wird geladen…