Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Anthraquinone | HCID 6780 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Quino(2,3-b)acridine-7,14-dione, 5,6,12,13-tetrahydro- | HCID 79973 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | Quinacridone | HCID 13976 | — |
Reaction Steps
A one liter flask equipped with a thermometer, stirrer and condenser is charged with 50 g 6,13-dihydroquinacridone, 200 ml methanol, 1 g polyvinyl pyrrolidone powder (Luviskole K-30, BASF) and 7 g of the aqueous presscake of the nanosize quinacridone naphthalene sulfonic acid formaldehyde polymer mixture according to Example 2 are stirred at 20-27° C. for 10 minutes. 50 g 50% aqueous sodium hydroxide are added. The mixture is stirred under a slow flow of nitrogen at 50-53° C. for one hour. 0.8 g anthraquinone mono sulfonic acid sodium salt is added as catalyst and the reaction mixture is heated to reflux for 10 minutes. 76 g of an aqueous 18.9% hydrogen peroxide solution are added into the reaction mixture with a peristaltic pump at a pumping rate of 0.4 ml/minute. Then after 25 minutes addition time 1.6 g phthalimidomethyl-quinacridone are introduced into the reaction mixture followed by continuing the hydrogen peroxide addition while maintaining reflux and a slow nitrogen flow. The resulting violet suspension is further stirred for 10 minutes at reflux then diluted with 100 ml cold water and filtered. The presscake is washed with hot water then dried, yielding a small particle size violet beta quinacridone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06864371B2 |
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| Source dataset | uspto-grants-2005_03 |
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| ORD ID | ord-f653d5e768154dee9be98336386e70a4 |
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| Source note | uspto-grants-2005_03 |
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