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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399845Generated: October 30, 2026

Hydrochloric Acid → 3-(5-Aminopyrazol-1-yl)benzoic acid

https://huagongshe.com/reaction/399845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant5-amino-1-(3-carboxyphenyl)-1H-pyrazole-4-carboxylic acidHCID 18945399—
SolventWaterHCID 962—
SolventDiglymeHCID 8150—
Product3-(5-Aminopyrazol-1-yl)benzoic acidHCID 1894527547.6%

Reaction Steps

The mixture of 3-(5-amino-4-carboxypyrazol-1-yl)benzoic acid (19.4 g) in diglyme (200 ml) was heated under reflux for 6 hours. To the mixture was added a mixture of ethyl acetate and water, and adjusted to pH 9 with 20% aqueous potassium carbonate solution. The separated aqueous layer was adjusted to pH 3.5 with 6N-hydrochloric acid and the mixture was extracted with a solution of ethyl acetate and tetrahydrofuran. The extract layer was washed with brine, dried over magnesium sulfate and evaporated in vacuo to give 3-(5-aminopyrazol-1-yl)benzoic acid (7.59 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05824691
Source datasetuspto-grants-1998_10
ORD IDord-3f9c204d4be84050a73219bb4f0f3ae9
Source noteuspto-grants-1998_10