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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182254Generated: November 2, 2026

Sodium Hydroxide → 3-[(Phenylsulfonyl)amino]-2-thiophenecarboxylic acid

https://huagongshe.com/reaction/1182254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantmethyl 3-[(phenylsulfonyl)amino]thiophene-2-carboxylateHCID 4430392—
SolventAcetonitrileHCID 6342—
Product3-[(Phenylsulfonyl)amino]-2-thiophenecarboxylic acidHCID 1677809195%

Reaction Conditions

Temperature50 °C

Reaction Steps

3-Benzenesulfonylaminothiophene-2-carboxylic acid methyl ester (1.5 g, 5.0 mmol) was dissolved in acetonitrile (10 mL) and treated with aqueous, sodium hydroxide solution (2N, 7.5 mL, 3 equivalents) at room temperature. The solution was warmed to 50° C. and monitored by thin layer chromatography. Upon completion of the reaction, the mixture was cooled and extracted once with diethyl ether. The ether layer was set aside. The aqueous layer was then acidified with aqueous HCl (2N, excess) before re-extracting twice with ethyl acetate. The combined organic layers were washed once with brine solution and dried over anhydrous sodium sulfate. The ethyl acetate was decanted and evaporated under reduced pressure to give of 3-benzenesulfonylaminothiophene-2-carboxylic acid (1.34 g, 95%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288538B2
Source datasetuspto-grants-2007_10
ORD IDord-bd9a0798d0ad4eb6b944f69005b9728b
Source noteuspto-grants-2007_10