HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-(2-fluoro-5-nitrophenyl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Fluoro-5-nitroaniline | HCID 67785 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2-fluoro-5-nitrophenyl)methanesulfonamide | HCID 4416401 | 75.2% |
Reaction Steps
To 1300 ml of a pyridine solution containing 204.0 g of 2-fluoro-5-nitroaniline was added 165.0 g of methanesulfonyl chloride under ice cooling, followed by stirring at room temperature for 24 hours. To the reaction solution was added 3000 ml of water, and the precipitate was collected by filtration, air-dried overnight and recrystallized from ethanol to give 230.0 g of N-(2-fluoro-5-nitrophenyl)methanesulfonamide as colorless needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05374764 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-6fe0c93e16794f3a96c4bdc8230d2fd8 |
| Source note | uspto-grants-1994_12 |