Acetic Acid → N-Acetyl-2,6-xylidine
Reaktionsgleichung
[NH2:1][C:2]1[C:3]([CH3:9])=[CH:4][CH:5]=[CH:6][C:7]=1[CH3:8].[C:10](OC(=O)C)(=[O:12])[CH3:11].C(O)(=O)C>O>[C:10]([NH:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][C:3]=1[CH3:9])(=[O:12])[CH3:11]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To 25 ml of 2,6-xylidine (0.20 mole) was added slowly a mixture of 25 ml of acetic anhydride (0.26 mole) and 25 ml of acetic acid (0.44 mole) under stirring at room temperature. The mixture was stirred for 30 minutes at room temperature and, then, diluted with water. The crystalline precipitate was collected by filtration to give 30.1 g (91%) of the title compound (m.p. 182°-184° C.; colorless needles).
Aufarbeitung
- stirringThe mixture was stirred for 30 minutes at room temperature
- filtrationThe crystalline precipitate was collected by filtration
Quellen und Nachweise
- ORD-Eintrag
- ord-65932ea602734fb29d525f9b6ee3ee14
- Quelldatensatz
- uspto-grants-1988_06
- Patentnummer
- US04751232
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