Ammonia → 7-Bromoquinolin-5-ol
反応式
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][CH:8]=[N:9]2)=[C:4]([O:12]C)[CH:3]=1.Br.N>O>[OH:12][C:4]1[CH:3]=[C:2]([Br:1])[CH:11]=[C:10]2[C:5]=1[CH:6]=[CH:7][CH:8]=[N:9]2参加物
5
実験手順
1.5 g (0.0064 mol) of 7-bromo-5-methoxy-quinoline were refluxed with 48% HBr (30 ml) for 20 h. After cooling to room temperature reaction mixture was poured into 100 ml of water and basified with saturated ammonia solution. Product was filtered off, washed with water and dried at 50° C. in vacuo. Yield of 7-bromo-5-hydroxy-quinoline was 600 mg (41%).
後処理
- customreaction mixture
- filtrationProduct was filtered off
- washwashed with water
- customdried at 50° C. in vacuo
出典と根拠
- ORDレコード
- ord-28981c1d283947eaa84e8e876f62703f
- 出典データセット
- uspto-grants-2014_12
- 特許番号
- US08912173B2
反応ノート
読み込み中…