反応式
[F:1][CH:2]=[C:3]([F:5])[F:4].[CH:6]1[C:11]([NH2:12])=[CH:10][CH:9]=[C:8]([OH:13])[CH:7]=1.[OH-].[K+]>CN(C=O)C>[F:4][C:3]([F:5])([O:13][C:8]1[CH:9]=[CH:10][C:11]([NH2:12])=[CH:6][CH:7]=1)[CH2:2][F:1]参加物
5
実験手順
Gaseous trifluoroethylene was bubbled into a mixture of 7.0 g (64.1 mmol) of p-aminophenol, 0.7 g (12.8 mmol) of powdered KOH, and 70 ml dry DMF at 90° C. for 11/4 hours. The mixture was poured into ice water and extracted 2 times with ether. The combined ether layers were washed with diluted aqueous NaOH, washed with water, dried over MgSO4 and filtered. HCl was bubbled into the ether solution. The resulting gray solid was collected by filtration to give 3.6 g (25 percent of theoretical) of the above-named aniline as the HCl salt along with a 20 percent impurity of 4-(1,2-difluoroethenyloxy)benzene-amine.
後処理
- extractionextracted 2 times with ether
- washThe combined ether layers were washed with diluted aqueous NaOH
- washwashed with water
- dry with materialdried over MgSO4
- filtrationfiltered
- customHCl was bubbled into the ether solution
- filtrationThe resulting gray solid was collected by filtration
出典と根拠
- ORDレコード
- ord-b6d402b15d8b4fe29491860fc02ae96b
- 出典データセット
- uspto-grants-1993_10
- 特許番号
- US05250690
関連ノート
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