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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626725Generated: November 3, 2026

Hydrochloric Acid → 5-Chloro-2-({[3-(furan-3-yl)phenyl]carbonyl}amino)benzoic acid

https://huagongshe.com/reaction/1626725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 5-chloro-2-({[3-(furan-3-yl)phenyl]carbonyl}amino)benzoateHCID 66680385—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-2-({[3-(furan-3-yl)phenyl]carbonyl}amino)benzoic acidHCID 4693555441%

Reaction Conditions

Temperature50 °C

Reaction Steps

0.61 g (1.7 mmol) of methyl 5-chloro-2-({[3-(furan-3-yl)phenyl]carbonyl}amino)benzoate was dissolved in 20 mL of THF solvent, and 4 mL of 1N aqueous sodium hydroxide was added. The mixture was stirred at 50° C. for 1.5 hours. After cooling, 1N hydrochloric acid was added to acidify the reaction mixture. Thereafter, the solvent was distilled off under reduced pressure. Subsequently, water was added to the residue, and solids were collected by filtration and washed with water. The obtained crude product was recrystallized using a mixed solvent of ethyl acetate and n-hexane, thereby giving 0.24 g of the target 5-chloro-2-({[3-(furan-3-yl)phenyl]carbonyl}amino)benzoic acid (yield: 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785473B2
Source datasetuspto-grants-2014_07
ORD IDord-38c31f20f81e485ab7bbb80efb220d58
Source noteuspto-grants-2014_07