Cyanuric chloride → Anthraquinone

HRID 1196099Notes

Reaction equation

HRID 1196099 reaction equation
N[C:2]1[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7](=[O:17])[C:6]=2[C:5](SC2C=CC(S(O)(=O)=O)=CC=2)=[CH:4][C:3]=1OC1C=CC(S(O)(=O)=O)=C(N)C=1.N1C(Cl)=NC(Cl)=NC=1Cl.NC1C=C(S(O)(=O)=O)C=CC=1>>[CH:9]1[C:8]2[C:7](=[O:17])[C:6]3[C:15](=[CH:2][CH:3]=[CH:4][CH:5]=3)[C:14](=[O:16])[C:13]=2[CH:12]=[CH:11][CH:10]=1

Participants

4

Reactant 3

HCID 7954Cyanuric chlorideHCID 84743-Aminobenzenesulfonic acidHCID 147173781-Amino-2-(3'-amino-4'-sulfophenoxy)-4-(4-sulfophenylthio)anthraquinone

Product 1

HCID 6780Anthraquinone

Procedure

Example 11 was repeated, provided that the shown in 1st, 2nd and 3rd columns of the following table were used in place of the 1-amino-2-(3'-amino-4'-sulfophenoxy)-4-(4'-sulfophenylthio)anthraquinone, cyanuric chloride and 3-aminobenzenesulfonic acid, respectively, thereby obtaining a corresponding anthraquinone compound. The color shade obtained by dyeing cotton with the compound is as shown in a 4th column of the table.

Workup

  1. customprovided that the

Sources & evidence

ORD record
ord-6195ab31858749238e4d0fdf361fa239
Source dataset
uspto-grants-1992_05
Patent number
US05112971

Reaction notes

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