2-Acetylbutyrolactone → HCID 178432037, Verbindung
Reaktionsgleichung
Br.[NH2:2][C:3]1[NH:7][N:6]=[C:5]([CH3:8])[C:4]=1[Br:9].[C:10]([CH:13]1[CH2:18][CH2:17][O:16][C:14]1=[O:15])(=O)[CH3:11]>C(O)C>[Br:9][C:4]1[C:5]([CH3:8])=[N:6][N:7]2[C:14]([OH:15])=[C:13]([CH2:18][CH2:17][OH:16])[C:10]([CH3:11])=[N:2][C:3]=12Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 5-amino-4-bromo-3-methylpyrazole hydrobromide (13 g, 51 mmol) and α-acetyl-γ-butyrolactone (6.8 g, 53 mmol) in ethanol (65 mL) was heated under reflux for nine hours. After cooling to room temperature, the resulting crystals were collected by filtration, to give the title compound (4.6 g) as white crystals.
Aufarbeitung
- temperatureunder reflux for nine hours
- filtrationthe resulting crystals were collected by filtration
Quellen und Nachweise
- ORD-Eintrag
- ord-301fb18165de450c9d1f7329c9ad1eec
- Quelldatensatz
- uspto-grants-2005_10
- Patentnummer
- US06951865B2
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