1-Amino-4-bromo-9,10-dioxo-9,10-dihydroanthracene-2-carboxylic acid → Anthraquinone
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](Br)=[CH:4][C:3]=1C(O)=O.OCCS(C1C=CC(OC2C=CC(S)=CC=2)=CC=1)(=O)=O>>[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]=1Participants
3
Procedure
Example 19 was repeated, except that the compounds shown in 1st and 2nd columns of the following table were used in place of the 1-amino-2-carboxy-4-bromoanthraquinone and 4-(4'-β-hydroxyethylsulfonylphenoxy)thiophenol, respectively, thereby obtaining a corresponding anthraquinone compound. The color shade obtained by dyeing cotton with the compound is as shown in a 3rd column of the table.
Sources & evidence
- ORD record
- ord-6b9b3cf3204347f3a0bd89387565066d
- Source dataset
- uspto-grants-1993_11
- Patent number
- US05266696
Reaction notes
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