反応式
[Cl:1][C:2]1[C:10]([Cl:11])=[C:9]([O:12][C:13]([F:16])([F:15])[F:14])[CH:8]=[CH:7][C:3]=1[C:4](F)=[O:5].[OH2:17]>>[Cl:1][C:2]1[C:10]([Cl:11])=[C:9]([O:12][C:13]([F:16])([F:15])[F:14])[CH:8]=[CH:7][C:3]=1[C:4]([OH:17])=[O:5]参加物
3
実験手順
A suspension of crude 2,3-dichloro-4-trifluoromethoxybenzoyl fluoride (2 g, containing mixed antimony halides) in water was stirred vigorously for 24 hours. The mixture was extracted with dichloromethane and filtered. The organic layer was washed with hydrochloric acid (2M), aqueous sodium chloride solution and extracted into sodium carbonate solution (2M). The aqueous extract was acidified to pH1 and the solid was filtered off and washed with water to give 2,3-dichloro-4-trifluoromethoxybenzoic acid (0.6 g) as a white solid mp123°-126° C.
後処理
- extractionThe mixture was extracted with dichloromethane
- filtrationfiltered
- washThe organic layer was washed with hydrochloric acid (2M), aqueous sodium chloride solution
- extractionextracted into sodium carbonate solution (2M)
- extractionThe aqueous extract
- filtrationthe solid was filtered off
- washwashed with water
出典と根拠
- ORDレコード
- ord-c1322224a8f54c50bfc3d63890ce33e2
- 出典データセット
- uspto-grants-1997_07
- 特許番号
- US05650533
関連ノート
読み込み中…