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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841595Generated: October 26, 2026

Water → N-(4-hydroxy-phenyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide

https://huagongshe.com/reaction/1841595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2777399—
Reactantp-(N-methylamino)phenol sulfateHCID 10198132—
SolventTolueneHCID 1140—
ProductN-(4-hydroxy-phenyl)-N-methyl-4-trifluoromethyl-benzenesulfonamideHCID 23446603100.4%

Reaction Steps

13.8 g (40 mmol) of 4-methylaminophenol hemisulfate (twice suspended in toluene and evaporated under reduced pressure to remove water) were suspended in 100 ml hexamethyldisilazane and refluxed for 2.5 h. The solution was evaporated under reduced pressure and dissolved in 270 ml THF. 9.79 g (40 mmol) of 4-(trifluoromethyl)benzenesulfonyl chloride were added slowly at 0° C. and the reaction mixture was stirred for 16 h at room temperature. 30 ml H2O were added and after 1 h the solvents were evaporated. The residue was extracted with water/Et2O (3×), the organic phases were washed with 10% NaCl, dried (Na2SO4) and evaporated to yield 13.3 g (100%) of N-(4-hydroxy-phenyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide, mp: 145-146° C.; MS: 331 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06683201B2
Source datasetuspto-grants-2004_01
ORD IDord-7371c4166a0c4115b4dddc7db14df458
Source noteuspto-grants-2004_01