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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606608Generated: October 29, 2026

Hydrochloric Acid → 2-(5-Carboxyfurfurylamino)-4-chloro-5-methylsulfonylbenzoic acid

https://huagongshe.com/reaction/1606608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
Reactant51521-75-6HCID 22101365—
Reactant5-(Aminomethyl)furan-2-carboxylic acid hydrochlorideHCID 56807544—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventTriethylamineHCID 8471—
Product2-(5-Carboxyfurfurylamino)-4-chloro-5-methylsulfonylbenzoic acidHCID 21543963—

Reaction Steps

A mixture of 2,4-dichloro-5-methylsulfonylbenzoic acid (3.50 g.; 0.013 mole), 5-aminomethyl-2-furancarboxylic acid hydrochloride (4.83 g.; 0.027 mole), triethylamine (11.5 ml.), and glyme (25 ml.) is heated to 140°-150° C. for 24 hours. Solid sodium bicarbonate (5.0 g.) is added and refluxing is continued for another 24 hours. The mixture is poured into water (150 ml.) and acidified by the addition of 6N hydrochloric acid. The tan solid is collected, washed with water, and dried, 1.20 g., m.p. 269°-272° C. Recrystallization from acetonitrile gives 2-(5-carboxyfurfurylamino)-4-chloro-5-methylsulfonylbenzoic acid, m.p. 263.5°-265.5° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03953476
Source datasetuspto-grants-1976_04
ORD IDord-373033f9ef074426958868561f9e26ad
Source noteuspto-grants-1976_04