反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH2:11])(=[O:10])=[O:9])=[CH:4][CH:3]=1.[Cl:12][CH2:13][C:14](Cl)=[O:15]>>[Cl:12][CH2:13][C:14]([NH:11][S:8]([C:5]1[CH:4]=[CH:3][C:2]([Cl:1])=[CH:7][CH:6]=1)(=[O:9])=[O:10])=[O:15]参加物
3
実験手順
The reactant N-chloroacetyl 4-chlorobenzene sulfonamide was prepared by mixing 30.0 g of 4-chlorobenzene sulfonamide and 60.0 ml of chloroacetylchloride. The mixture was refluxed for 6 hours, allowed to cool, and stand at room temperature overnight. The crystalline product was removed by filtration, washed repeatedly with hexane, and dried. The product consisted of 32.5 g of reactant (m.p. 122°-124° C.). Structure was confirmed by IR and NMR.
後処理
- temperatureThe mixture was refluxed for 6 hours
- temperatureto cool
- customThe crystalline product was removed by filtration
- washwashed repeatedly with hexane
- customdried
出典と根拠
- ORDレコード
- ord-6ff650ebc91f4cc8b8beabbdb27ea031
- 出典データセット
- uspto-grants-1985_01
- 特許番号
- US04495365
関連ノート
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