反応式
[C:1]1([S:7](Cl)=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH3:10]>CCOCC>[C:1]1([S:7]([NH2:10])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
4
実験手順
Benzenesulphinamide was prepared by reacting benzenesulphinyl chloride with ammonia in ether initially at -78° C. and finally at ambient temperature and was isolated in 17% yield as a solid, m.p. 112°-115° C.
後処理
- custominitially at -78° C.
- customfinally at ambient temperature and was isolated in 17% yield as a solid, m.p. 112°-115° C.
出典と根拠
- ORDレコード
- ord-61f89b91a1154459a9933bf9d6056d4e
- 出典データセット
- uspto-grants-1991_03
- 特許番号
- US04997844
関連ノート
読み込み中…