HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxygen → 4-Methylphenyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 4-Methylphenyl acetate | HCID 8797 | — |
| Reactant | 1,3,5-Trihydroxy-1,3,5-triazinane-2,4,6-trione | HCID 10419723 | — |
| Catalyst | Cobalt diacetate | HCID 6277 | — |
| Catalyst | Manganous Acetate | HCID 12525 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Methylphenyl acetate | HCID 8797 | — |
| Product | Benzoic acid, 4-(acetyloxy)- | HCID 16865 | — |
Reaction Steps
A mixture of 0.300 g of p-tolyl acetate, 0.018 g of hexahydro-1,3,5-trihydroxy-1,3,5-triazine-2,4,6-trione (5% by mole relative to p-tolyl acetate), 5 g of acetic acid, 0.003 g of cobalt(II) acetate.4H2O, 0.001 g of manganese(II) acetate.4H2O and 0.003 g of 2,2′-azobisisobutyronitrile was stirred at 100° C. in an atmosphere of oxygene gas (1 atm=0.1 MPa) for 6 hours. The resulting product in the reaction mixture was analyzed by gas chromatography and was found to yield 4-acetoxybenzoic acid in 82% yield at 85% conversion of p-tolyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091342B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-6ceb42c45e9a4b67a98dfccbbdb747c4 |
| Source note | uspto-grants-2006_08 |