HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003355Generated: October 25, 2026
Sulfuric Acid → 3-Chloro-4-acetoxybenzoic acid
https://huagongshe.com/reaction/1003355
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Chloro-4-hydroxybenzoic acid hemihydrate | HCID 2723611 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | 3-Chloro-4-acetoxybenzoic acid | HCID 10656296 | 75% |
Reaction Steps
3-Chloro-4-hydroxybenzoic acid hemihydrate (10.16 g, 56 mmol) was dissolved in 20 ml of acetic anhydride, followed by the addition of 0.5 ml of concentrated sulfuric acid. The resulting mixture was stirred at 100° C. for 3 hours and was then allowed to stand overnight at room temperature. The precipitate was collected by filtration and then washed with benzene, whereby 8.95 g of 4-acetoxy-3-chlorobenzoic acid were obtained (yield: 75%, melting point: 149-151° C.). A mixture of 8.95 g (41.7 mmol) of 4-acetoxy-3-chlorobenzoic acid and 22.23 g (167 mmol) of aluminum chloride was then heated at 180° C. for 3 hours. Subsequent to the addition of ice and 1N hydrochloric acid, the resultant mixture was extracted with ethyl acetate. The organic layer was washed with water and was then dried over MgSO4. The solvent was distilled off under reduced pressure and the residue was recrystallized from ethyl acetate, whereby 2.97 g of the title compound were obtained as yellow powder (yield: 33%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06046212 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-4743a01007e14990be8d0b7dc4a33db6 |
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| Source note | uspto-grants-2000_04 |
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