HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Anthraquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | 2-Benzyltoluene | HCID 69738 | — |
| Catalyst | Cobalt diacetate | HCID 6277 | — |
| Catalyst | Manganous Acetate | HCID 12525 | — |
| Catalyst | Cobalt dibromide | HCID 24610 | — |
| Product | Anthraquinone | HCID 6780 | — |
Reaction Steps
The reactor described in Example 1 is charged with a mixture of 60.7 g o-benzyl-toluene (5/8 Mol), 607 ml dry acetic acid, 3 g cobalt (II) acetate.4H2O, 0.5 g manganese (II) acetate.4H2O and 3.0 g cobalt (II) bromide.6H2O. The reaction is carried out as described above. The uptake of oxygen is completed after about 3 hours. After the analogous work up 2.2 g anthraquinone (3.2% of theory) and 68.1 g crude o-benzoyl-benzoic acid (90.4% of theory) are recovered; the acid number approaches 226, and the color is medium brown. Heating of a small sample with concentrated sulfuric acid yields a darkly-colored anthraquinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04185023 |
| Source dataset | uspto-grants-1980_01 |
| ORD ID | ord-7aa3c5defc4d4509a66317727b452ac5 |
| Source note | uspto-grants-1980_01 |