Reaktionsgleichung
[C:1]([CH2:4][C:5](=O)[CH3:6])(=O)[CH3:2].[NH2:8][C:9]([NH2:11])=[O:10].[ClH:12]>C(O)C>[ClH:12].[CH3:2][C:1]1[CH:4]=[C:5]([CH3:6])[NH:11][C:9](=[O:10])[N:8]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
To a mixture of acetyl acetone (4.0 g, 40.0 mmol) and urea (2.0 g, 33.3 mmol) in ethanol (40 mL) was added concentrated HCl (10 mL) and stirred at reflux for 3 h. The reaction mixture was cooled to 0° C. and filtered; the colourless solid was washed thoroughly with ice cold ethanol then ether and dried under vacuum to afford 4,6-dimethyl-1H-pyrimidin-2-one hydrochloride (3.5 g, 55%) as a solid.
Aufarbeitung
- temperatureat reflux for 3 h
- filtrationfiltered
- washthe colourless solid was washed thoroughly with ice cold ethanol
- dry with materialether and dried under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-491904216b374f63a45fd8b8a8d40266
- Quelldatensatz
- uspto-grants-2013_12
- Patentnummer
- US08604029B2
Verknüpfte Notizen
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