反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([C:11]([S:16]([C:19]2[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][CH:20]=2)(=[O:18])=[O:17])=[CH:12]OCC)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[F:26][C:27]([F:36])([F:35])[C:28]1[CH:34]=[CH:33][CH:32]=[CH:31][C:29]=1[NH2:30]>CC(N(C)C)=O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([S:8]([C:11]([S:16]([C:19]2[CH:20]=[CH:21][C:22]([Cl:25])=[CH:23][CH:24]=2)(=[O:18])=[O:17])=[CH:12][NH:30][C:29]2[CH:31]=[CH:32][CH:33]=[CH:34][C:28]=2[C:27]([F:26])([F:35])[F:36])(=[O:10])=[O:9])=[CH:6][CH:7]=1参加物
4
実験手順
A solution of 1,1-bis(4-chlorophenylsulphonyl)-2-ethoxyethene (1.26 g) and 2-(trifluoromethyl)aniline (0.48 g) in dimethylacetamide (20 ml) was heated at reflux for 2 hours, and then it was cooled and poured onto ice (50 g). The resulting white precipitate was filtered off, washed with water and recrystallised from ethanol, to give 1,1-bis(4-chlorophenylsulphonyl)-2-[2-(trifluoromethyl)anilino]ethene (0.8 g), m.p. 169°-171° C.
後処理
- temperatureat reflux for 2 hours
- temperatureit was cooled
- additionpoured onto ice (50 g)
- filtrationThe resulting white precipitate was filtered off
- washwashed with water
- customrecrystallised from ethanol
出典と根拠
- ORDレコード
- ord-603f45c2fba84f72880705f9baeb8a82
- 出典データセット
- uspto-grants-1987_04
- 特許番号
- US04659727
関連ノート
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