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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398971Generated: October 30, 2026

4-Aminobenzoic Acid → 4-[(3-Methyl-1,2-oxazole-5-carbonyl)amino]benzoic acid

https://huagongshe.com/reaction/2398971

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminobenzoic AcidHCID 978—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Methyl-1,2-oxazole-5-carbonyl chlorideHCID 12905099—
SolventAcetoneHCID 180—
Product4-[(3-Methyl-1,2-oxazole-5-carbonyl)amino]benzoic acidHCID 2143222773.7%

Reaction Steps

To a stirred suspension of 6.9g of p-aminobenzoic acid and 3.5 g of potassium carbonate in 60 ml of acetone was added 7.3 g of 3-methylisoxazole-5-carbonyl chloride. The mixture was stirred at room temperature for 1 hr. and then refluxed for 1 hr. The precipitate was filtered off and dissolved in water. The solution was acidified with concentrated hydrochloride acid. The precipitate was filtered off and washed with ethanol. There was obtained 9.1 g of N-(p-carboxyphenyl)-3-methylisoxazole-5-carboxamide. Melting point: above 300° C. Yield: 73.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04026902
Source datasetuspto-grants-1977_05
ORD IDord-3ef31d1a859c46f79597e24cc5a20b64
Source noteuspto-grants-1977_05