Potassium Hydroxide → HCID 21824655、化合物
反応式
[OH:1][C:2]1[C:11]2[N:10]=[C:9]([CH3:12])[CH:8]=[CH:7][C:6]=2[C:5]([S:13]([OH:16])(=[O:15])=[O:14])=[CH:4][CH:3]=1.[OH-].[K+].[Cl:19][O-].[Na+]>O>[Cl:19][C:3]1[CH:4]=[C:5]([S:13]([OH:16])(=[O:15])=[O:14])[C:6]2[CH:7]=[CH:8][C:9]([CH3:12])=[N:10][C:11]=2[C:2]=1[OH:1]参加物
実験手順
8-Hydroxy-2-methyl-quinoline-5-sulfonic acid (14.0 g, 58.52 mmol) was added to a solution of potassium hydroxide (9.20 g, 164 mmol, 2.8 equiv) in water (136 ml) to form a yellow solution. An aqueous solution of sodium hypochlorite (13%, 136 ml) was added. The mixture was stirred at room temperature for 90 minutes. Upon dilution with water (300 ml), the mixture was filtered through amberlite IR-120 (H+). After washing the column with water (2 liters), the eluent was concentrated (to ˜200 ml) and diluted with acetone (300 ml). The precipitate was filtered off and washed with acetone to afford the title compound (5.51 g, 34%). 1H NMR (400 MHz, d6-DMSO): δ=8.52 (d, J=8.3 Hz, 1H), 7.67 (d, J=8.3 Hz, 1H), 7.00 (s, 1H), 2.58 (s, 3H). MS (ES−): 274 (M−H)−.
後処理
- customto form a yellow solution
- filtrationUpon dilution with water (300 ml), the mixture was filtered through amberlite IR-120 (H+)
- washAfter washing the column with water (2 liters)
- concentrationthe eluent was concentrated (to ˜200 ml)
- additiondiluted with acetone (300 ml)
- filtrationThe precipitate was filtered off
- washwashed with acetone
出典と根拠
- ORDレコード
- ord-e5b9df65fd464b49bea4816626dba80d
- 出典データセット
- uspto-grants-2013_04
- 特許番号
- US08426440B2
反応ノート
読み込み中…