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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072402Generated: November 1, 2026

Methacrylic Acid → N-(p-aminosulfonylphenyl)methacrylamide

https://huagongshe.com/reaction/1072402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethacrylic AcidHCID 4093—
ReactantSulfanilamideHCID 5333—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductN-(p-aminosulfonylphenyl)methacrylamideHCID 35006265.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a 500 ml volume three-necked flask equipped with a stirring machine, a cooling tube and a dropping funnel, there were added 31.0 g (0.36 mole) of methacrylic acid, 39.1 g (0.36 mole) of ethyl chloroformate and 200 ml of acetonitrile and then the resulting mixture was stirred while cooling it in an ice-water bath. To this mixture, there was dropwise added 36.4 g (0.36 mole) of triethylamine through the dropping funnel over about one hour. After the completion of the dropwise addition, the ice-water bath was removed and the mixture was stirred at room temperature for 30 minutes. To this reaction mixture, there was added 51.7 g (0.30 mole) of p-aminobenzene sulfonamide and the resulting mixture was stirred over one hour while warming the mixture at 70° C. in an oil bath. After the completion of the reaction, the mixture was introduced into 1 L of water while stirring the water and the resulting mixture was stirred for 30 minutes. This mixture was filtered to recover the precipitates, followed by addition of 500 ml of water to the precipitates to give a slurry, filtration of the slurry and drying the resulting solid to give N-(p-aminosulfonylphenyl)methacrylamide as a white solid (yield 46.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06911299B2
Source datasetuspto-grants-2005_06
ORD IDord-d94ddb0cac504318bfbecc6ce470255a
Source noteuspto-grants-2005_06