Reaktionsgleichung
[CH3:1][N:2]([CH3:12])/[C:3](=[C:5]1\[N:6]=[C:7]([CH3:11])[O:8][C:9]\1=[O:10])/[CH3:4].[H-].[Na+].[CH2:15]([OH:17])[CH3:16]>>[CH2:15]([O:17][C:9](=[O:10])/[C:5](/[NH:6][C:7](=[O:8])[CH3:11])=[C:3](/[N:2]([CH3:12])[CH3:1])\[CH3:4])[CH3:16]Komponenten
4
Versuchsvorschrift
4-[1-Dimethylamino-eth-(Z)-ylidene]-2-methyl-4H-oxazol-5-one (36.4 g, 216 mmol) was dissolved in ethanol (300 ml) and sodium hydride (0.52 g, 0.022 mmol) was added at room temperature. The dark solution was refluxed for 1 h. The solvent was evaporated and the crude product [MS: m/e=215.5 (M+H+)] was used without any further purification for the next step.
Aufarbeitung
- temperatureThe dark solution was refluxed for 1 h
- customThe solvent was evaporated
- customthe crude product [MS: m/e=215.5 (M+H+)] was used without any further purification for the next step
Quellen und Nachweise
- ORD-Eintrag
- ord-212504e11fa94b00bf4bfb4a4eca3fe8
- Quelldatensatz
- uspto-grants-2006_08
- Patentnummer
- US07091222B2
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