Ammonia → 2-Methyl-3-(phenylmethoxy)-4(3H)-pyridinone
Reaktionsgleichung
[NH3:1].[CH2:2]([O:9][C:10]1[C:15](=[O:16])[CH:14]=[CH:13]O[C:11]=1[CH3:17])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>C(O)C>[CH2:2]([O:9][CH:10]1[C:15](=[O:16])[CH:14]=[CH:13][N:1]=[C:11]1[CH3:17])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
28% aqueous ammonia (100 ml) and 30 ml of ethanol were added to 3-benzyloxy-2-methyl-4-pyrone (40.6 g, 0.188 mol). The mixture was stirred at room temperature for 5 days. The reaction mixture was concentrated under the reduced pressure. The precipitate was filtered, and was then washed with a minor amount of ethyl acetate to give 32.2 g of 3-benzyloxy-2-methyl-4-pyridone as a light yellow crystal. The same compound was also obtained from the filtrate (5.6 g, yield 93%).
Aufarbeitung
- concentrationThe reaction mixture was concentrated under the reduced pressure
- filtrationThe precipitate was filtered
- washwas then washed with a minor amount of ethyl acetate
Quellen und Nachweise
- ORD-Eintrag
- ord-b6e6b19f184240c9a58a1a91aad130b7
- Quelldatensatz
- uspto-grants-2007_02
- Patentnummer
- US07183278B1
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