HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257289Generated: October 26, 2026
Acetic Acid → 4-(Acetyloxy)-3-tert-butylbenzoic acid
https://huagongshe.com/reaction/257289
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-tert-Butyl-4-methylphenol | HCID 17004 | — |
| Catalyst | Hydrogen Bromide | HCID 260 | — |
| Catalyst | Cobalt diacetate | HCID 6277 | — |
| Catalyst | Manganese dibromide | HCID 6432071 | — |
| Product | 4-(Acetyloxy)-3-tert-butylbenzoic acid | HCID 18007736 | 84.4% |
Reaction Steps
A mixture of 82.0 g of 2-tert-butyl-4-methylphenol, 140.0 g of acetic anhydride and 3.0 g of hydrobromic acid (48%) is heated at 90° C. for 1 hour. 280.0 g of acetic acid, 2.5 g of cobalt(II) acetate (tetrahydrate) and 2.5 g of manganese(II) bromide (tetrahydrate) are added, and oxygen (30 ml/min) is passed through the solution at 110° C. The acetic acid is partially removed by applying a vacuum. The reaction mixture which remains is poured into 500 ml of water and filtered, giving 99.5 g (84%) of the product in the form of colourless crystals having a melting point of from 180° to 182° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05261953 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-27fce9cf87e94677ab6c77efa7f38b23 |
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| Source note | uspto-grants-1993_11 |
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