反応式
[N+](C1C=C(S(O)(=O)=O)C(C)=CC=1)([O-])=O.[N+:15]([C:18]1[CH:19]=[C:20]([S:39]([OH:42])(=[O:41])=[O:40])[C:21]([CH:24]=[CH:25][C:26]2[C:27]([S:35]([OH:38])(=[O:37])=[O:36])=[CH:28][C:29]([N+:32]([O-])=O)=[CH:30][CH:31]=2)=[CH:22][CH:23]=1)([O-])=O.O=O>>[NH2:15][C:18]1[CH:19]=[C:20]([S:39]([OH:42])(=[O:41])=[O:40])[C:21]([CH:24]=[CH:25][C:26]2[C:27]([S:35]([OH:38])(=[O:37])=[O:36])=[CH:28][C:29]([NH2:32])=[CH:30][CH:31]=2)=[CH:22][CH:23]=1参加物
4
実験手順
Furthermore, 4-nitrotoluene-2-sulphonic acid can be used for the preparation of 4,4'-dinitrostilbene-2,2'-disulphonic acid, in which, for example, an approximately 30 to 50% strength aqueous solution of 4-nitrotoluene-2-sulphonic acid is reacted with oxidizing agents, for example with atmospheric oxygen. 4,4'-Dinitrostilbene-2,2'-disulphonic acid can be further processed by reduction to give 4,4'-diaminostilbene-2,2'-disulphonic acid (see Ber. 30, 3,100), and is an important intermediate product for the preparation of optical brighteners (A. Dorlars, C.-W. Schellhammer and J. Schroeder, Angew. Chem. 87, 693 (1975)).
出典と根拠
- ORDレコード
- ord-0f5d053ff31a48c282883c354f88544b
- 出典データセット
- uspto-grants-1983_05
- 特許番号
- US04382039
関連ノート
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