Hydroxylamine, O-ethyl- → HCID 178474708, Verbindung
Reaktionsgleichung
[C:1]([CH:4]1[C:9](=[O:10])[N:8]([CH3:11])[C:7](=[O:12])[N:6]([CH3:13])[C:5]1=[O:14])(=O)[CH3:2].[CH2:15]([O:17][NH2:18])[CH3:16]>C(O)C>[CH2:15]([O:17][NH:18][C:1](=[C:4]1[C:9](=[O:10])[N:8]([CH3:11])[C:7](=[O:12])[N:6]([CH3:13])[C:5]1=[O:14])[CH3:2])[CH3:16]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 40 °C
Versuchsvorschrift
1.5 g of 5-acetyl-1,3-dimethylbarbituric acid was dissolved in 50 ml of ethanol and 1.5 ml of ethoxyamine was added to it. After the resulting solution was stirred at 40° C during 2 hours, it was allowed to stand at a room temperature. The separated white plates were filtered and recrystallized from ethanol, and thereby 1.4 g of the desired compound was obtained.
Aufarbeitung
- customto stand at a room temperature
- filtrationThe separated white plates were filtered
- customrecrystallized from ethanol
Quellen und Nachweise
- ORD-Eintrag
- ord-dd0ace17155e40818c433d3d4cdd945c
- Quelldatensatz
- uspto-grants-1976_12
- Patentnummer
- US03999974
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