Benzene → HCID 21312565, Verbindung
Reaktionsgleichung
[CH2:1]([C:3]1([CH2:12][CH3:13])[C:8](=[O:9])[NH:7][C:6](=[O:10])[NH:5][C:4]1=[O:11])[CH3:2].Cl[CH2:15][CH2:16][CH2:17][C:18]([O:20][CH3:21])=[O:19].[C:22](=[O:25])([O-])[O-:23].[K+].[K+].[CH:28]1[CH:33]=CC=C[CH:29]=1.[CH3:34]N(C)C=O>>[CH3:21][O:20][C:18]([CH2:17][CH2:16][CH2:15][N:7]1[C:8](=[O:9])[C:3]([CH2:1][CH3:2])([CH2:12][CH3:13])[C:4](=[O:11])[N:5]([CH2:29][CH2:28][CH2:33][C:22]([O:23][CH3:34])=[O:25])[C:6]1=[O:10])=[O:19]Komponenten
6
Versuchsvorschrift
18.4 g (0.1 mol) of 5,5-diethylbarbituric acid are reacted with 28.7 g (0.21 mol) of methyl γ-chlorobutyrate according to Example 1. 15.2 g (0.11 mol) of potassium carbonate powder are used as the acid acceptor and 100 ml of benzene and 100 ml of dimethylformamide are used as the solvent. The reaction is carried out exactly according to Example 1 and likewise worked up. In this manner, 38.3 g (99.7% of theory) of a clear, slightly discoloured viscous product are obtained.
Aufarbeitung
- customIn this manner, 38.3 g (99.7% of theory) of a clear, slightly discoloured viscous product are obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-38018ddc63f14eb8b330d469b9e561c9
- Quelldatensatz
- uspto-grants-1979_07
- Patentnummer
- US04161603
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