HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → Quinacridone
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
10 Parts of the 6,13-dihydroquinacridone obtained in Example 9 and 80 parts of methanol were charged into a 200-ml flask having a refluxer, and 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. 40 Parts of 10% sulfuric acid was added dropwise to hydrolyze the salt, and the reaction mixture was refluxed under for 1 hour. 10 Parts of sodium m-nitrobenzenesulfonate was added, and the mixture was refluxed for 4 hours to give 9.76 parts (98.2% of the theoretical yield) of an unsubstituted quinacridone having an excellent particle diameter as a pigment.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05817817 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-d6633d6c04b641ee94b6f2415663560f |
| Source note | uspto-grants-1998_10 |