HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-(2,5-difluorophenyl)-4-methylbenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 2,5-Difluoroaniline | HCID 67775 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(2,5-difluorophenyl)-4-methylbenzenesulfonamide | HCID 8500594 | 76.1% |
Reaction Steps
A stirred mixture of 15.0 g (0.116 mole) of 2,5-difluoroaniline and 24.4 g (0.128 mole) of 4-methylphenylsulfonyl chloride in 50 ml of pyridine was heated at reflux for approximately 18 hours. The reaction mixture was cooled and poured into 500 ml of 6N hydrochloric acid. This acidic mixture was allowed to stand at room temperature for two days. A precipitate formed and was collected by filtration. The filter cake was washed with dilute hydrochloric acid and was dried under reduced pressure to yield 25.0 g of N-(4-methylphenylsulfonyl)-2,5-difluoroaniline. The nmr spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05310724 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-1ce6795f8a0e4167b6ecbfdfe83df79a |
| Source note | uspto-grants-1994_05 |