HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4-tert-Butylbenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-tert-Butyltoluene | HCID 7390 | — |
| Catalyst | Cobalt(II) acetate tetrahydrate | HCID 61372 | — |
| Catalyst | Sodium Bromide | HCID 253881 | — |
| Product | 4-tert-Butylbenzoic acid | HCID 7403 | 86.4% |
Reaction Steps
Analogously to Example 1, 300 g of p-tert-butyltoluene (93.3% pure) was oxidized in the presence of 50 g of acetic acid, 3 g of cobalt acetate tetrahydrate and 1.5 g of sodium bromide at 25 bar and 115°-135° C. by passing air through it to produce a gas exhaust rate of 1.5 liters per minute. The oxygen absorption ended after a reaction period of 300 minutes; then 450 g of 74.5% acetic acid was added, the dilute reaction mixture was cooled with stirring to room temperature and filtered, and the crystallizate was washed with 450g of 70% acetic acid. 311.5 g of p-tert-butylbenzoic acid resulted, in the form of white crystals of a purity of 99.6 percent by weight as determined by gas chromatography, with a terephthalic acid content of 0.16%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04603220 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-ce0a3f85e58a4eb1b31c67e6762ef737 |
| Source note | uspto-grants-1986_07 |