反应方程式
[OH:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([S:13]([OH:16])(=[O:15])=[O:14])=[CH:9][C:10]=2[NH2:12])[CH:5]=[C:4]([S:17]([OH:20])(=[O:19])=[O:18])[CH:3]=1.[Cl:21][C:22]1[N:27]=[C:26](Cl)[N:25]=[C:24]([Cl:29])[N:23]=1>O>[OH:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([S:13]([OH:16])(=[O:15])=[O:14])=[CH:9][C:10]=2[NH:12][C:26]2[N:25]=[C:24]([Cl:29])[N:23]=[C:22]([Cl:21])[N:27]=2)[CH:5]=[C:4]([S:17]([OH:20])(=[O:19])=[O:18])[CH:3]=1参与物
4
反应条件
- 温度
- 2.5 °C
实验过程
An ice cold neutral solution of 1-hydroxy-8-aminonaphthalene-3,6-disulphonic acid (31.9 parts) in water (120 parts) was added, with stirring, to a freshly prepared suspension of 2,4,6-trichloro-s-triazine (18.5 parts) in ice and water (140 parts). The mixture was stirred for 3 hours at 0 to 5° C. to give a solution of 1-hydroxy-8-(2,4-dichloro-s-triazin-6-ylamino-)naphthalene-3,6-disulphonic acid (solution 1).
来源与证据
- ORD记录
- ord-96c6ea8add314387a32fb0ab620e9b4d
- 来源数据集
- uspto-grants-2000_05
- 专利号
- US06068667
关联笔记
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