Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | 2,5-Dianilinoterephthalic acid | HCID 82351 | — |
| Reactant | 1,4-Benzenedicarboxylic acid, 2,5-bis[(3-chlorophenyl)amino]- | HCID 119916 | — |
| Reactant | HCID 53655966 | HCID 53655966 | — |
| Product | Quinacridone | HCID 13976 | — |
Reaction Steps
465 parts of polyphosphoric acid, containing 85.0% P2O5, are introduced into a pressure vessel. Then 83.8 parts of 2,5-dianilinoterephthalic acid, 4.6 parts of 2,5-di(3-toluidino)terephthalic acid and 4.6 parts of 2,5-di(3-chloro-anilino)terephthalic acid are introduced with stirring at from 80 to 90° C. and the mixture is heated at 125° C. for 1 hour during which ring closure takes place to form the quinacridone. The reaction mixture is then introduced into a second pressure vessel where it is hydrolyzed under pressure and with stirring with a mixture of 2095 parts of 30% phosphoric acid at 140° C. During this hydrolysis the temperature rises to 155° C. The mixture is stirred at 155° C. for 0.5 hour. Then it is cooled to 60° C. and the mixed crystal pigment is filtered off with suction, washed to neutrality with water and dried at 80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05989333 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-e1a40cefb2504e998ef8c8af01841a33 |
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| Source note | uspto-grants-1999_11 |
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