Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 10954793 | HCID 10954793 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Aminoanthraquinone | HCID 6710 | — |
Reaction Steps
200 g of a paste which contains 95 g of 4-aminoanthrone and also contains sulphuric acid, and which is obtained in accordance with the instructions of Example 2, are suspended in 1 l of water and neutralized with concentrated sodium hydroxide solution, and the 4-aminoanthrone is filtered off. It is equally possible to start from the corresponding amount of 4-aminoanthrone which has been obtained according to Example 5 or 6. The 4-aminoanthrone is now stirred into 1 l of water, 150 ml of potassium waterglass (d = 1.25) are added, the mixture is warmed to 60° C and 500 ml of 6% strength hydrogen peroxide solution are added dropwise in the course of 2 hours. This causes the color of the suspension to change from yellow to red. The mixture is stirred for a further 3 hours and is filtered, and the residue is washed until neutral. After drying, 100 g of 1-aminoanthraquinone of 90% purity (89% of theory) are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04006170 |
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| Source dataset | uspto-grants-1977_02 |
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| ORD ID | ord-b2fe1ce7f12443378f673a3f73efbc7a |
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| Source note | uspto-grants-1977_02 |
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