Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Diaminoanthraquinone | HCID 15652 | — |
| Reactant | HCID 23462634 | HCID 23462634 | — |
| Product | Anthraquinone | HCID 6780 | — |
Reaction Steps
Instead of using a unitary diaminoanthraquinone of the formula (2) it is also possible to use a mixture of diaminoanthraquinones, for example a mixture of 1,5-, 1,6- and 1,7-diaminoanthraquinone. Mixtures of the diaminoanthraquinones which are formed in the industrial manufacture of diaminoanthraquinones by dinitration of anthraquinone and subsequent reduction are particularly suitable. Such mixtures contain for example small amounts of 2,7- and 2,8-diaminoanthraquinone (β-isomers) and 1-aminoanthraquinone in addition to the 1,8-, 1,5-, 1,7- and 1,6-diaminoanthraquinones principally obtained, or they contain small amounts of 1-aminoanthraquinone, 2-aminoanthraquinone and 1-amino-2-, -4-, -5- and -8-hydroxyanthraquinone in addition to 1,6-, 1,8-, 1,7-, 2,6-, 2,7- and 1,5-diaminoanthraquinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04265633 |
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| Source dataset | uspto-grants-1981_05 |
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| ORD ID | ord-62f0f3dfe5b149e2ac7c2db3d7173477 |
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| Source note | uspto-grants-1981_05 |
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