Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | p-Acetylphenyl acetate | HCID 83063 | — |
| Product | Benzoic acid, 4-(acetyloxy)- | HCID 16865 | 73% |
Reaction Steps
The oxidation of p-acetoxyacetophenone proceeded as in Example I, except that the reaction was run for 30 minutes and a total of 150 g (1.47 moles) of acetic anhydride and 37 g (0.62 mole) of acetic acid was added through the pump. The reaction mixture was concentrated from 772 g to 413 g by evaporation of acetic acid. The slurry was filtered to remove precipitated p-acetoxybenzoic acid. After drying, 128.2 g of p-acetoxybenzoic acid of 95 mole % purity (73% yield) were obtained. Remaining in the filtrate were: p-acetoxybenzoic acid, 8.5 mole % yield, p-acetoxyacetophenone, 1.8 mole % yield, p-hydroxybenzoic acid, 0.6 mole % yield. Analysis of the reactor wash showed 2.6 mole % p-acetoxybenzoic acid. Total reaction yield of p-acetoxybenzoic acid was 84 mole %.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04873361 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-de40f7f7f1614b808ef8daf65461d46c |
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| Source note | uspto-grants-1989_10 |
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