HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoic acid, 4-(acetyloxy)- → 4'-Hydroxyacetophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoic acid, 4-(acetyloxy)- | HCID 16865 | — |
| Reactant | p-Acetylphenyl acetate | HCID 83063 | — |
| Product | 4'-Hydroxyacetophenone | HCID 7469 | — |
Reaction Steps
The 4-acetoxyacetophenone (4-AAP) used as the starting material for the catalytic oxidation to 4-acetoxybenzoic acid may be obtained as a co-product with the 4-hydroxyacetophenone (4-HAP) produced by the Fries rearrangement of phenyl acetate or the Friedel-Crafts acetylation of phenol, e.g., when the reaction is carried out in the presence of HF and an acid anhydide, or it may be produced from the 4-HAP by reacting the latter with an acetylating agent such as acetic anhydride, as indicated by equation (III), by contacting the 4-HAP with, for example, about 1 to 5 moles of the anhydride per mole of 4-HAP at a temperature, for example, in the range of 120° to 140° C. for a period, for example, in the range of 1 to 4 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04665215 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-b2761c3277664900868a91d0c8f671bf |
| Source note | uspto-grants-1987_05 |