Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium 3-nitrobenzenesulfonate | HCID 31389 | — |
| Reactant | Quino(2,3-b)acridine-7,14-dione, 5,6,12,13-tetrahydro- | HCID 79973 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Quinacridone | HCID 13976 | — |
Reaction Steps
A stainless steel flask having a refluxing device was charged with 10 parts of the 6,13-dihydroquinacridone obtained in Example 1 and 80 parts of methanol, and the mixture was stirred. 12 Parts of a 50% NaOH aqueous solution was added, and the mixture was stirred at 40° C. for 30 minutes to form a salt. 26 Parts of 10% sulfuric acid was added to hydrolyze the salt, and the resultant solution was refluxed for 1 hour. Then, 10 parts of sodium m-nitrobenzenesulfonate was added, and immediately thereafter, 3 parts of a 50% NaOH aqueous solution was added. Then, the mixture was refluxed for 4 hours to give 9.8 parts (98.8% of a theoretical value) of a nonsubstituted quinacridone as a pigment having a uniform particle diameter. The so-obtained quinacridone had a specific surface area of 25.1 m2 /g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05610306 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-3920c5e846a04297b75c2c75c822ecfe |
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| Source note | uspto-grants-1997_03 |
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