Ethanol → 2-(3-Bromo-5-methoxyphenyl)acetic acid
反応式
[Br:1][C:2]1[CH:3]=[C:4]([O:11][CH3:12])[CH:5]=[C:6](CC#N)[CH:7]=1.[OH-:13].[Na+].[CH2:15]([OH:17])[CH3:16]>>[Br:1][C:2]1[CH:3]=[C:4]([O:11][CH3:12])[CH:5]=[C:6]([CH2:16][C:15]([OH:13])=[O:17])[CH:7]=1参加物
4
実験手順
A mixture of 5-bromo-3-methoxyphenylacetonitrile (22.6 g, 0.1 m) and 10% aqueous sodium hydroxide (300 ml) in ethanol (225 ml) is heated to 95° for 18 hours. The mixture is concentrated in vacuo, acidified with 10% hydrochloric acid and extracted with ethyl acetate. The ethyl acetate extract is washed, dried with sodium sulfate and concentrated in vacuo to give 5-bromo-3-methoxyphenylacetic acid.
後処理
- temperatureis heated to 95° for 18 hours
- concentrationThe mixture is concentrated in vacuo
- extractionextracted with ethyl acetate
- extractionThe ethyl acetate extract
- washis washed
- dry with materialdried with sodium sulfate
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-f8d8aac79f9944a39050130b8f950566
- 出典データセット
- uspto-grants-1989_04
- 特許番号
- US04824839
反応ノート
読み込み中…