Ammonium Hydroxide → 4-Methyl-2-phenyloxazole-5-carboxamide
Reaktionsgleichung
[OH-].[NH4+:2].[C:3]([C:8]1[O:12][C:11]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[N:10][C:9]=1[CH3:19])(OCC)=[O:4]>C(O)C>[C:3]([C:8]1[O:12][C:11]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[N:10][C:9]=1[CH3:19])(=[O:4])[NH2:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
150 Ml. (2.5 mole) of concentrated ammonium hydroxide is added dropwise to a solution of 10 g. (0.0434 mole) of 5-carbethoxy-2-phenyl-4-methyloxazole in 150 ml. of 95% ethanol. The mixture is stirred three days at room temperature, then it is concentrated to 50 ml. by evaporating the ethanol and chilled. The precipitated product is filtered, washed, dried over sodium sulfate and recrystallized from methanol; yield 3.7 g. of the title compound; m.p. 187°-190°.
Aufarbeitung
- concentrationit is concentrated to 50 ml
- customby evaporating the ethanol
- temperaturechilled
- filtrationThe precipitated product is filtered
- washwashed
- dry with materialdried over sodium sulfate
- customrecrystallized from methanol
Quellen und Nachweise
- ORD-Eintrag
- ord-41a18a3b133e47a28f4c0d53ffcb7d5b
- Quelldatensatz
- uspto-grants-1978_02
- Patentnummer
- US04072689
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