Benzene → HCID 21312565、化合物
反応式
[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]参加物
6
実験手順
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.
後処理
- customIn this manner, 38.3 g (99.7% of theory) of a clear, slightly discoloured viscous product are obtained
出典と根拠
- ORDレコード
- ord-38018ddc63f14eb8b330d469b9e561c9
- 出典データセット
- uspto-grants-1979_07
- 特許番号
- US04161603
反応ノート
読み込み中…