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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942450Generated: October 26, 2026

Acetic Anhydride → 4-(Acetyloxy)-3-nitrobenzoic acid

https://huagongshe.com/reaction/1942450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-Hydroxy-3-nitrobenzoic acidHCID 12033—
SolventPyridineHCID 1049—
Product4-(Acetyloxy)-3-nitrobenzoic acidHCID 14057307—

Reaction Steps

To 4-hydroxy-3-nitrobenzoic acid (10 g) were added pyridine (12 ml) and acetic anhydride (55 ml), and the mixture was stirred at room temperature for 65 hours. The reaction solution was concentrated under reduced pressure, and thereto was added a 5% aqueous sodium hydrogen sulfate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and concentrated under reduced pressure to give the title compound (11.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389511B2
Source datasetuspto-grants-2013_03
ORD IDord-08f9aeba1a974cd8b246e3d336654e04
Source noteuspto-grants-2013_03