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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395597Generated: October 25, 2026

Triethylamine → N-{4-[(4-hydroxyphenyl)(methyl)sulfamoyl]phenyl}acetamide

https://huagongshe.com/reaction/395597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-Acetylsulfanilyl chlorideHCID 8481—
Reactantp-(N-methylamino)phenol sulfateHCID 10198132—
SolventEthanolHCID 702—
ProductN-{4-[(4-hydroxyphenyl)(methyl)sulfamoyl]phenyl}acetamideHCID 2998367—

Reaction Steps

4-Methylaminophenol sulfate and equivalent 4-acetamidobenzenesulfonyl chloride and double equivalent triethylamine were reacted in ethanol at room temperature for 4 hours. After the solvent was removed in vacuo, the residue was extracted with diethyl ether. The ether layer was washed successively with 2 N hydrochloric acid, saturated aqueous NaHCO3 solution and water, then dried over anhydrous Na2SO4 The solvent was removed and the residue was recrystallized from ethanol to give N-(4-hydroxyphenyl)-N-methyl-4-acetamidobenzenesulfonamide, mp 202-203° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605635B1
Source datasetuspto-grants-2003_08
ORD IDord-c49085fcab17466c95941101e1a3525b
Source noteuspto-grants-2003_08