反応式
[OH-].[Na+].[O:3]=[C:4]1[CH2:12][CH2:11][CH2:10][C:9]2[NH:8][CH:7]=[CH:6][C:5]1=2.[C:13]1([S:19](Cl)(=[O:21])=[O:20])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>ClCCCl>[C:13]1([S:19]([N:8]2[C:9]3[CH2:10][CH2:11][CH2:12][C:4](=[O:3])[C:5]=3[CH:6]=[CH:7]2)(=[O:21])=[O:20])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1参加物
反応条件
- 温度
- 0 °C
実験手順
To a suspension of NaOH (4.44 g) in 1,2-dichloroethane (250 mL) was added 4-oxo-4,5,6,7-tetrahydroindole (5.0 g). The mixture was then cooled to 0° C. and stirred for 30 min, following which a solution of phenylsulfonyl chloride (5.7 mL) in 1,2-dichloroethane (50 mL) was added dropwise over a period of 30 min. After 30 min of stirring, the reaction mixture was allowed to come to room temperature and stirred overnight. The reaction was quenched by pouring onto distilled water (100 mL). The organic layer was separated, and the aqueous layer was extracted with dichloromethane (3×50 mL). The combined organic extract was washed with distilled water to neutrality, dried over MgSO4, and concentrated in vacuo to afford 7.0 g of the title compound.
後処理
- additionwas added dropwise over a period of 30 min
- stirringAfter 30 min of stirring
- customto come to room temperature
- stirringstirred overnight
- customThe reaction was quenched
- additionby pouring
- distillationonto distilled water (100 mL)
- customThe organic layer was separated
- extractionthe aqueous layer was extracted with dichloromethane (3×50 mL)
- extractionThe combined organic extract
- washwas washed with distilled water to neutrality
- dry with materialdried over MgSO4
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-db1be117db264d6aa8a894f8482557ef
- 出典データセット
- uspto-grants-2011_02
- 特許番号
- US07884109B2
関連ノート
読み込み中…