Ethyl Acrylate → Ethyl 1-benzyl-5-(1,3-dithiol-2-ylidene)-4,6-dioxopiperidine-3-carboxylate
反応式
[H-].[Na+].[S:3]1[CH:7]=[CH:6][S:5][C:4]1=[C:8]([C:14](=[O:23])[NH:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[C:9]([O:11]CC)=O.[C:24]([O:28][CH2:29][CH3:30])(=[O:27])[CH:25]=[CH2:26]>CN(C)C=O>[CH2:16]([N:15]1[C:14](=[O:23])[C:8](=[C:4]2[S:3][CH:7]=[CH:6][S:5]2)[C:9](=[O:11])[CH:25]([C:24]([O:28][CH2:29][CH3:30])=[O:27])[CH2:26]1)[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1参加物
実験手順
Sodium hydride (a 60% dispersion in oil) (1.50 g) is suspended in N,N-dimethylformamide (100 ml) and a solution of ethyl 2-(1,3-dithiol-2-ylidene)-2-(N-benzylcarbamoyl)acetate (10.0 g) in dimethylformamide (250 ml) is added dropwise thereto at 4° to 5° C. The mixture is stirred at the same temperature for 30 minutes. A solution of ethyl acrylate (4.1 ml) in dimethylformamide (100 ml) is added dropwise to the mixture, and the mixture is stirred at the same temperature for one hour and then at room temperature for 5 hours. The mixture is poured into ice-water, and the aqueous solution is extracted with ethyl acetate. The extract is washed with water, dried and then evaporated to remove the solvent. The residue is recrystallized from a mixture of n-hexane and ethyl acetate, whereby ethyl 1-benzyl-5-(1,3-dithiol-2-ylidene)-4,6-dioxopiperidine-3-carboxylate (8.76 g ) is obtained as pale yellow needles. Yield: 75%.
後処理
- customat 4° to 5° C
- stirringthe mixture is stirred at the same temperature for one hour
- waitat room temperature for 5 hours
- extractionthe aqueous solution is extracted with ethyl acetate
- washThe extract is washed with water
- customdried
- customevaporated
- customto remove the solvent
- customThe residue is recrystallized from a mixture of n-hexane and ethyl acetate
出典と根拠
- ORDレコード
- ord-80759b6916004bb7bbee9c74aca4efa6
- 出典データセット
- uspto-grants-1987_05
- 特許番号
- US04663319
反応ノート
読み込み中…