HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604868Generated: November 1, 2026
4-Hydroxybenzoic Acid → Benzoic acid, 4-(acetyloxy)-
https://huagongshe.com/reaction/1604868
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Hydroxybenzoic Acid | HCID 135 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Product | Benzoic acid, 4-(acetyloxy)- | HCID 16865 | — |
Reaction Steps
For example, 500 grams of acetic anhydride and 2 drops of sulfuric acid are placed in a vessel and 274 grams of p-hydroxy benzoic acid are added with stirring. The contents of the vessel are stirred at 100°C. for 1 hour, and are cooled to about 15°C. The p-acetoxy benzoic acid formed is recovered by pouring the hot acetic anhydride solution over an ice/water mixture, removing the product by filtration, washing the same with deionized water in a high shear mixer, and drying in a forced air oven. A like quantity of m-acetoxy benzoic acid is formed in an identical manner utilizing m-hydroxy benzoic acid as one of the reactants.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03948856 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-63b5d5d9e1c9424c929f9a38cd950901 |
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| Source note | uspto-grants-1976_04 |
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