Reaktionsgleichung
[CH2:1]([O:3][C:4](=[O:10])[C:5](OCC)=[NH:6])[CH3:2].[C:11]1([CH2:17][C:18]([NH:20][NH2:21])=O)[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.[CH2:22](O)[CH3:23]>>[CH2:1]([O:3][C:4]([C:5]1[N:6]=[C:18]([CH2:17][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[NH:20][N:21]=1)=[O:10])[CH2:2][CH2:22][CH3:23]Komponenten
4
Reaktionsbedingungen
- Temperatur
- 80 °C
Versuchsvorschrift
Ethyl-2-ethoxy-2-iminoacetate (1.318 g, 9.08 mmol) and phenyl acetic acid hydrazide (1.364 g, 9.08 mmol) were mixed together in ethanol (20 ml) and stirred at 80° C. for 1 h. Ethanol was evaporated. The residue was dissolved in n-butanol (20 ml). The reaction mixture was stirred at 150° C. for 20 h, then solvents were evaporated.
Aufarbeitung
- customEthanol was evaporated
- dissolutionThe residue was dissolved in n-butanol (20 ml)
- stirringThe reaction mixture was stirred at 150° C. for 20 h
- customsolvents were evaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-12d0f595110f482ea4f4751a12afcd85
- Quelldatensatz
- uspto-grants-2016_03
- Patentnummer
- US09290485B2
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