反応式
[NH2:1][C:2]1[CH:11]=CC2[C:4](=CC(S(O)(=O)=O)=CC=2O)[C:3]=1[S:17]([OH:20])(=[O:19])=[O:18].FC1N=NN=C(F)C=1F.N1[CH2:35][CH2:34][O:33][CH2:32]C1>>[NH2:1][C:2]1[CH:11]=[C:35]([S:17]([OH:20])(=[O:19])=[O:18])[C:34]([O:33][CH3:32])=[CH:4][C:3]=1[S:17]([OH:20])(=[O:19])=[O:18]参加物
4
実験手順
31.9 g of 2-amino-5-hydroxy-naphthalene-1,7-disulphonic acid are subjected to a condensation reaction with trifluorotriazine and then with morpholine as described in Example 1. A diazo compound obtained by the customary route by direct diazotisation of 28.3 g of 1-amino-4-methoxy-benzene-2,5-disulphonic acid is added to the resulting suspension of the monofluorotriazinyl compound at 5°-10°, the pH simultaneously being kept at 7.0-7.5 by sprinkling in sodium bicarbonate. When the coupling has ended, the dyestuff of the formula ##STR19## is salted out, filtered off with suction, dried and ground. The red dyestuff powder dissolves readily in water and dyes cotton a brilliant reddish-tinged orange (colour code number 5).
出典と根拠
- ORDレコード
- ord-59e36a8e775243849756eae2477d615a
- 出典データセット
- uspto-grants-1995_10
- 特許番号
- US05459246
関連ノート
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