Methanol → 3-Fluoroquinolin-7-OL
反応式
[F:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[C:7]([O:12]C)[CH:6]=2.B(Br)(Br)Br.CO>ClCCl>[F:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[C:7]([OH:12])[CH:6]=2参加物
5
実験手順
3-Fluoro-7-methoxyquinoline (130 mg, 0.74 mmol) was taken up in dichloromethane (2 ml) under nitrogen and treated with boron tribromide (4 ml of a 11.0M solution of in dichloromethane). The reaction mixture was stirred for 24 hours at ambient temperature followed by quenching the reaction by the slow addition of excess methanol. The solution was stirred for a further 2 hours and evaporated to dryness to give 3-fluoro-7-hydroxyquinoline which was used without further purification.
後処理
- customby quenching
- customthe reaction
- stirringThe solution was stirred for a further 2 hours
- customevaporated to dryness
出典と根拠
- ORDレコード
- ord-76e7e2024c9c4fb4b22242708b9a260b
- 出典データセット
- uspto-grants-2006_07
- 特許番号
- US07074800B1
反応ノート
読み込み中…