HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloroanthraquinone → Anthrimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloroanthraquinone | HCID 6709 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Disperse Violet 1 | HCID 31420 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | Anthrimide | HCID 6700 | — |
Reaction Steps
Following the procedure as descrilbed in Example 1, but suspending the 1-chloroanthraquinone, 1,4-diaminoanthraquinone, sodium carbonate and CuCl in 300 ml of nitrobenzene, the anthrimide is obtained in a yield corresponding to that of Example 1. When following a conventional procedure, i.e. mixing the components and heating them slowly, if such a concentrated reaction mixture is employed, the reaction can no longer be carried out in an agitator vessel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04701281 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-a3d0b1a6bb41422fb40fef4e3f3f4b93 |
| Source note | uspto-grants-1987_10 |