Water → Diethyl 2-Amino-2-(4-Octylphenethyl)malonate
反応式
[H-].[Na+].[CH2:3]([O:5][C:6]([CH:8]([CH2:14][CH2:15][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])=[CH:18][CH:17]=1)[C:9]([O:11][CH2:12][CH3:13])=[O:10])=[O:7])[CH3:4].[N+:30](C1C=C([N+]([O-])=O)C=CC=1ON)([O-])=O.O>CN(C)C=O>[NH2:30][C:8]([C:9]([O:11][CH2:12][CH3:13])=[O:10])([CH2:14][CH2:15][C:16]1[CH:17]=[CH:18][C:19]([CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])=[CH:20][CH:21]=1)[C:6]([O:5][CH2:3][CH3:4])=[O:7]参加物
6
実験手順
60% Sodium hydride (0.38 g) was suspended in dry dimethyl-formamide (30 ml) and ethyl 2-ethoxycarbonyl-4-(4-octylphenyl)-butyrate (3.0 g) was added thereto. The mixture was stirred at room temperature for 2 hours. O-(2,4-Dinitrophenyl)hydroxyl-amine (1.14 g) was added thereto and the mixture was stirred at room temperature for 5 hours. The reaction mixture was poured into cool water and extracted with toluene. The extract was washed with aqueous sodium chloride and dried over magnesium sulfate. The solvent was distilled away under reduced pressure to give 3 g of the subject compound.
後処理
- stirringthe mixture was stirred at room temperature for 5 hours
- additionThe reaction mixture was poured
- extractionextracted with toluene
- washThe extract was washed with aqueous sodium chloride
- dry with materialdried over magnesium sulfate
- distillationThe solvent was distilled away under reduced pressure
出典と根拠
- ORDレコード
- ord-b7b0dae6e6ba4da2ab840cf29a0d3279
- 出典データセット
- uspto-grants-1999_09
- 特許番号
- US05952316
反応ノート
読み込み中…