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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003356Generated: October 31, 2026

Sulfuric Acid → 3-Acetoxybenzoic acid

https://huagongshe.com/reaction/1003356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant3-Hydroxybenzoic AcidHCID 7420—
ReactantAcetic AnhydrideHCID 7918—
Product3-Acetoxybenzoic acidHCID 238669—

Reaction Conditions

Temperature60 °C

Reaction Steps

Concentrated sulfuric acid (0.2 ml) was added to a solution of 10.07 g (72.9 mol) of 3-hydroxybenzoic acid in 10 ml of acetic anhydride. The resulting mixture was stirred at 60° C. for 1 hour and was then allowed to stand overnight at room temperature. The resulting precipitate was collected by filtration, washed with benzene, and then dried in air. The precipitate was recrystallized from acetone-hexane, whereby 8.92 g of 3-acetoxybenzoic acid were obtained as colorless prisms (yield: 67.9%, melting point: 149-151° C.). A mixture of 8.92 g (49.5 mmol) of 3-acetoxybenzoic acid and 26.33 g (198 mmol) of aluminum chloride was then heated at 160° C. for 3 hours. Subsequent to the addition of ice and 1N hydrochloric acid, the resulting mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride and was then dried over MgSO4. The solvent was distilled off under reduced pressure. The residue was recrystallized from ethanol, whereby 1.61 g of the title compound were obtained as pale yellow powder (yield: 18%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06046212
Source datasetuspto-grants-2000_04
ORD IDord-4be2263b36b443e391b5533f38af85ae
Source noteuspto-grants-2000_04