HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyromellitic dianhydride → Quinoline Yellow
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyromellitic dianhydride | HCID 6966 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | 4-Quinolinecarboxylic acid, 3-hydroxy-2-methyl- | HCID 67024 | — |
| Product | Quinoline Yellow | HCID 6731 | — |
Reaction Steps
65.4 Parts of pyromellitic acid dianhydride and 61 parts of 3-hydroxy-2-methyl-quinoline-4-carboxylic acid are heated under reflux at 205° in 1000 parts of nitrobenzene for 1 hour, distilling off the water produced by the reaction. The mixture is held at this temperature for 31/2 hours. The mixture is then cooled to 10° and after stirring at this temperature for 1 hour, is filtered and the product is washed in toluene and ethanol. 93 parts of a dark brown quinophthalone intermediate result.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04838943 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-015c8398cdb946a08c45db66e11f6834 |
| Source note | uspto-grants-1989_06 |