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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351787Generated: November 2, 2026

Acetic Acid → Benzoic acid, 4-(acetyloxy)-

https://huagongshe.com/reaction/2351787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetic AnhydrideHCID 7918—
Reactantp-Acetylphenyl acetateHCID 83063—
ProductBenzoic acid, 4-(acetyloxy)-HCID 1686573%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873361
Source datasetuspto-grants-1989_10
ORD IDord-de40f7f7f1614b808ef8daf65461d46c
Source noteuspto-grants-1989_10