Isatin → 1-Benzylisatin
反応式
[NH:1]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:4](=[O:5])[C:2]1=[O:3].[H-].[Na+].[CH2:14](Br)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>CN(C)C=O>[CH2:14]([N:1]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:4](=[O:5])[C:2]1=[O:3])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1参加物
実験手順
A solution of 44 g of isatin in 200 ml of N,N-dimethylformamide was added dropwise to a suspension of 16.0 g of sodium hydride (60%) in 100 ml of N,N-dimethylformamide at 0° C. in a nitrogen stream. After the mixture was stirred at that temperature for 30 minutes, a solution of 61.5 g of benzyl bromide in 100 ml of N,N-dimethylformamide was added thereto. The whole mixture was stirred for 1 hour and then concentrated. Chloroform was added to the residue, and the mixture was washed with saturated aqueous sodium hydrogencarbonate. The organic layer was dried over anhydrous sodium sulfate and concentrated. The resulting crude product was washed with hexane and recrystallized from ethanol to give 47.3 g (67%) of the title compound as red needles.
後処理
- stirringThe whole mixture was stirred for 1 hour
- concentrationconcentrated
- additionChloroform was added to the residue
- washthe mixture was washed with saturated aqueous sodium hydrogencarbonate
- dry with materialThe organic layer was dried over anhydrous sodium sulfate
- concentrationconcentrated
- washThe resulting crude product was washed with hexane
- customrecrystallized from ethanol
出典と根拠
- ORDレコード
- ord-01b6cbc3b8d7471d9087e2483e57e61e
- 出典データセット
- uspto-grants-2000_02
- 特許番号
- US06031111
反応ノート
読み込み中…