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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 4-(Trifluoromethyl)benzenesulfonyl chloride | HCID 2777399 | — |
| Reactant | p-(N-methylamino)phenol sulfate | HCID 10198132 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(4-hydroxy-phenyl)-N-methyl-4-trifluoromethyl-benzenesulfonamide | HCID 23446603 | 100.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06683201B2 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-7371c4166a0c4115b4dddc7db14df458 |
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| Source note | uspto-grants-2004_01 |
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