Ethanol → 4-Chloro-3,7-dimethylindole-2-carboxylic acid

HRID 361611ノート

反応式

HRID 361611 の反応式
[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

  1. temperatureThe reaction mixture was refluxed for 4 hours
  2. concentrationThe solution was concentrated
  3. addition1N HCl aqueous solution was added
  4. customThe precipitates were separated by filtration
  5. dissolutiondissolved in 50 ml of diethyl ether
  6. extractionextracted with 30 ml of aqueous sodium hydrogencarbonate solution three times
  7. washThe extract was washed with 30 ml of diethyl ether
  8. extractionextracted with 30 ml of diethyl ether three times
  9. dry with materialThe extract was dried over anhydrous magnesium sulfate
  10. 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

読み込み中…