Hydrochloric Acid → 4-Bromo-6-methoxyquinoline-3-carboxylic acid
反応式
[Br:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([O:12][CH3:13])[CH:10]=2)[N:5]=[CH:4][C:3]=1[C:14]([O:16]CC)=[O:15].[OH-].[Na+].Cl>C1COCC1>[Br:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([O:12][CH3:13])[CH:10]=2)[N:5]=[CH:4][C:3]=1[C:14]([OH:16])=[O:15]参加物
5
実験手順
To a solution of the ethyl 4-bromo-6-(methyloxy)-3-quinolinecarboxylate (12 g, 38.7 mmol) in THF (120 mL) was added 2N NaOH (45 mL, 90 mmol) dropwise over 15 min. The reaction solution was stirred for 24 h and then neutralized with 2N HCl (pH 6). The THF was removed in vacuo and the resulting aqueous solution was acidified to pH 2. The product was collected by filtration and washed with water and fully dried under vacuum (48 h). Isolated 10.8 g (100%).
後処理
- customThe THF was removed in vacuo
- filtrationThe product was collected by filtration
- washwashed with water
- customfully dried under vacuum (48 h)
- customIsolated 10.8 g (100%)
出典と根拠
- ORDレコード
- ord-fd7ccc8ad6a247368853a454134c76ac
- 出典データセット
- uspto-grants-2010_04
- 特許番号
- US07691850B2
反応ノート
読み込み中…