Hydrochloric Acid → 4-(4-Chloro-2-nitrophenoxy)benzoic acid
反応式
[Cl:1][C:2]1[CH:18]=[CH:17][C:5]([O:6][C:7]2[CH:16]=[CH:15][C:10]([C:11]([O:13]C)=[O:12])=[CH:9][CH:8]=2)=[C:4]([N+:19]([O-:21])=[O:20])[CH:3]=1.[Li+].[OH-].Cl>CO>[Cl:1][C:2]1[CH:18]=[CH:17][C:5]([O:6][C:7]2[CH:8]=[CH:9][C:10]([C:11]([OH:13])=[O:12])=[CH:15][CH:16]=2)=[C:4]([N+:19]([O-:21])=[O:20])[CH:3]=1参加物
5
実験手順
The compound from Example 126a (29.6 g, 96.2 mmol) in 200 mL of MeOH was treated with aqueous LiOH (1 M) and heated under reflux for 1 hour. Cooled to room temperature and acidified with aqueous HCl (1 M). Precipitate was filtered, washed with H2O and air-dried giving the title compound as a yellow solid (28.2 g, 100%).
後処理
- temperatureheated
- temperatureunder reflux for 1 hour
- filtrationPrecipitate was filtered
- washwashed with H2O
- customair-dried
出典と根拠
- ORDレコード
- ord-120f697c57074aa29560908f71c305ce
- 出典データセット
- uspto-grants-2012_12
- 特許番号
- US08338605B2
反応ノート
読み込み中…