6-methoxyquinoline-2-carboxylic Acid → 6-Hydroxyquinoline-2-carboxylic acid
反応式
C[O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]=[C:8]([C:13]([OH:15])=[O:14])[CH:7]=[CH:6]2>Br>[OH:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]=[C:8]([C:13]([OH:15])=[O:14])[CH:7]=[CH:6]2参加物
3
実験手順
6-Methoxy-2-quinolinecarboxylic acid (80.6 g) was refluxed in 48% hydrobromic acid (450 ml) for twenty-four hours. After cooling to room temperature, the solid was collected by filtration and then dissolved in water (1300 ml) at 90° and the pH of this solution was adjusted to 8-9 with concentrated ammonium hydroxide. After cooling to room temperature, the pH of this solution was adjusted to 4-5 with acetic acid. The resulting 6-hydroxy-2-quinolinecarboxylic acid was collected by filtration and washed with water (400 ml); yield 70 g, m.p. 260°-261° (dec).
後処理
- filtrationthe solid was collected by filtration
- dissolutiondissolved in water (1300 ml) at 90°
- temperatureAfter cooling to room temperature
- filtrationThe resulting 6-hydroxy-2-quinolinecarboxylic acid was collected by filtration
- washwashed with water (400 ml)
出典と根拠
- ORDレコード
- ord-cfc72d50ee1f4a3fab94b2fb4445f645
- 出典データセット
- uspto-grants-1984_07
- 特許番号
- US04461896
反応ノート
読み込み中…