Participants
| Role | Name | HCID | Charge |
|---|
| 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
79 Parts of methanol and 12 parts of a 50% NaOH aqueous solution were fully stirred in a stainless steel flask having a refluxing device. 10 Parts of the 6,13-dihydroquinacridone obtained in Example 1 and 10 parts of sodium m-nitrobenzenesulfonate were gradually mixed with the above-prepared solution, and the mixture was refluxed at 70° to 75° C. for 3 to 5 hours. The reaction mixture was cooled to 40° C. and filtered, and the resultant cake was cleaned with hot water until a wash liquid became colorless and transparent, to give 9.77 parts (98.3% of a theoretical value) of a nonsubstituted quinacridone. The so-obtained quinacridone was measured by IR and absorbance to show 99.2% of quinacridone and 0.8% of 6,13-dihydroquinacridone. The quinacridone had a specific surface area of 22.1 m2 /g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05610306 |
|---|
| Source dataset | uspto-grants-1997_03 |
|---|
| ORD ID | ord-7a6cb096bbc042858e95bb8fa78f4e12 |
|---|
| Source note | uspto-grants-1997_03 |
|---|