Hydrogen Bromide → 2-Chloro-4-(4-hydroxyphenyl)pyridine hydrobromide
反応式
[Cl:1][C:2]1[CH:7]=[C:6]([C:8]2[CH:13]=[CH:12][C:11]([O:14]C)=[CH:10][CH:9]=2)[CH:5]=[CH:4][N:3]=1.[BrH:16]>>[BrH:16].[Cl:1][C:2]1[CH:7]=[C:6]([C:8]2[CH:9]=[CH:10][C:11]([OH:14])=[CH:12][CH:13]=2)[CH:5]=[CH:4][N:3]=1参加物
3
実験手順
A mixture of 2-chloro-4-(4-methoxyphenyl)pyridine (4.6 g) and 48% aqueous hydrobromic acid solution is heated under reflux for 3.5 hours and allowed to cool back to room temperature. The precipitate that appears is separated by filtration, washed with water and dried under reduced pressure to give 4.9 g of 2-chloro-4-(4-hydroxyphenyl)pyridine hydrobromide as a yellow solid used without further purification.
後処理
- temperatureis heated
- temperatureunder reflux for 3.5 hours
- customThe precipitate that appears is separated by filtration
- washwashed with water
- customdried under reduced pressure
出典と根拠
- ORDレコード
- ord-8f8d494fbdab474f8a02b5649782bc73
- 出典データセット
- uspto-grants-2011_12
- 特許番号
- US08076329B2
反応ノート
読み込み中…