Ethanol → 4-Chloro-3,7-dimethylindole-2-carboxylic acid
反応式
[Cl:1][C:2]1[CH:10]=[CH:9][C:8]([CH3:11])=[C:7]2[C:3]=1[CH:4]=[C:5]([C:12]([O:14]CC)=[O:13])[NH:6]2.[OH-].[K+].[CH2:19](O)C>O>[Cl:1][C:2]1[CH:10]=[CH:9][C:8]([CH3:11])=[C:7]2[C:3]=1[C:4]([CH3:19])=[C:5]([C:12]([OH:14])=[O:13])[NH:6]2参加物
5
実験手順
In 20 ml of ethanol and 5 ml of water were dissolved 1.50 g (6.0 mmol) of ethyl 4-chloro-7-methylindole-2-carboxylate and 0.5 g (9.0 mmol) of potassium hydroxide. The reaction mixture was refluxed for 4 hours. The solution was concentrated and then 1N HCl aqueous solution was added. The precipitates were separated by filtration, dissolved in 50 ml of diethyl ether and extracted with 30 ml of aqueous sodium hydrogencarbonate solution three times. The extract was washed with 30 ml of diethyl ether. The water layers were made acid with 1N HCl aqueous solution and extracted with 30 ml of diethyl ether three times. The extract was dried over anhydrous magnesium sulfate and concentrated to provide 0.91 g of beige crystals. Yield: 68%
後処理
- temperatureThe reaction mixture was refluxed for 4 hours
- concentrationThe solution was concentrated
- addition1N HCl aqueous solution was added
- customThe precipitates were separated by filtration
- dissolutiondissolved in 50 ml of diethyl ether
- extractionextracted with 30 ml of aqueous sodium hydrogencarbonate solution three times
- washThe extract was washed with 30 ml of diethyl ether
- extractionextracted with 30 ml of diethyl ether three times
- dry with materialThe extract was dried over anhydrous magnesium sulfate
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-73c82cc3ae974eb8ad2df65408101ee8
- 出典データセット
- uspto-grants-1999_02
- 特許番号
- US05866594
反応ノート
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