HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35497Generated: October 29, 2026
Hydrochloric Acid → N-methyl-2,4-dimethyl-5-(trifluoromethanesulfonamido)benzenesulfonamide
https://huagongshe.com/reaction/35497
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 13300558 | HCID 13300558 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-methyl-2,4-dimethyl-5-(trifluoromethanesulfonamido)benzenesulfonamide | HCID 13300559 | 74.5% |
Reaction Steps
A mixture of 2,4-dimethyl-5-(trifluoromethanesulfonamido)benzenesulfonyl chloride (1.5 g), a 40% aqueous soltution of methylamine (1 g) and water (20 ml) was stirred at room temperature and allowed to stand overnight at the same temperature. The resultant mixture was made acidic with 5% aqueous hydrochloric acid to precipitate an oily substance, which was then extracted with chloroform. The organic layer was washed with a 5% aqueous solution of hydrochloric acid and water in order and dried over anhydrous magnesium sulfate, followed by concentration. The residue was allowed to stand to give crytals, which were recrystallized from toluene to give 1.1 g of N-methyl-2,4-dimethyl-5-(trifluoromethanesulfonamido)benzenesulfonamide (Compound No. 29). M.P., 134.5°-135.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04767446 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-66aedee05ec645c69a89c17fb21802a0 |
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| Source note | uspto-grants-1988_08 |
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