Disperse Yellow 42 → Benzenesulfonamide, 4-[(4-ethoxyphenyl)amino]-N,N-dimethyl-3-nitro-

HRID 618596

Reaction equation

HRID 618596 reaction equation
[CH:1]1[CH:6]=[CH:5][C:4]([NH:7][C:8]2[CH:13]=[CH:12][C:11]([S:14]([NH:17][C:18]3C=CC=CC=3)(=[O:16])=[O:15])=[CH:10][C:9]=2[N+:24]([O-:26])=[O:25])=[CH:3][CH:2]=1.C1C(N)=[C:31]2[C:34](C3C(O)=CC(Br)=C(N)C=3C(=O)C2=C(O)C=1)=[O:35].[CH:48]1C=CC(NC2C=CC([OH2+])=C3C(C4C(C(=O)C=23)=C([N+]([O-])=O)C=CC=4[O-])=O)=CC=1>>[CH3:31][CH2:34][O:35][C:1]1[CH:6]=[CH:5][C:4]([NH:7][C:8]2[CH:13]=[CH:12][C:11]([S:14]([N:17]([CH3:48])[CH3:18])(=[O:16])=[O:15])=[CH:10][C:9]=2[N+:24]([O-:26])=[O:25])=[CH:3][CH:2]=1

Participants

4

Reactant 3

HCID 21201Disperse Yellow 42HCID 337749,10-Anthracenedione, 1,5-diamino-2-bromo-4,8-dihydroxy-HCID 10205790620241-76-3

Product 1

HCID 105414Benzenesulfonamide, 4-[(4-ethoxyphenyl)amino]-N,N-dimethyl-3-nitro-

Procedure

0.185 % C.I. Disperse Yellow 42; 0.122 % C.I. Disperse Red 91; 0.05 % C.I. Disperse Blue 56; 0.44 % C.I. Disperse Blue 77; and 3.5 % of the dispersion of the dispersion of Example 11 above.

Sources & evidence

ORD record
ord-e3448bab5f0d4022a834ca587501edf5
Source dataset
uspto-grants-1999_09
Patent number
US05955005

Linked notes

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