Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | 2,5-Dianilinoterephthalic acid | HCID 82351 | — |
| Reactant | 2,5-Di-p-toluidinoterephthalic acid | HCID 82524 | — |
| Product | Quinacridone | HCID 13976 | — |
Reaction Steps
383 parts of polyphosphoric acid, containing 85.0% P2O5, are introduced into a stirred vessel. Then 69.0 parts of 2,5-dianilinoterephthalic acid and 7.66 parts of 2,5-di(4-toluidino)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 stirred vessel where it is hydrolyzed with stirring with a mixture of 1725 parts of 30% phosphoric acid at 55° C. During this hydrolysis the temperature rises to 67° C. The mixture is stirred at 67° C. for 0.5 hour. Then it is cooled to 60° C. and the pigment is filtered off with suction, washed to neutrality with water and dried at 80° C. This gives 68.7 parts of pigment which is in the α-phase of unsubstituted quinacridone (FIG. 2). Table 1 reproduces the X-ray diffraction spectrum of FIG. 2 in digital form.
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-36801d6bcd84416fb56c06d97a5ee3b3 |
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| Source note | uspto-grants-1999_11 |
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