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 | 72.8% |
Reaction Steps
To 334 ml of a pyridine solution containing 52.1 g of 2-fluoro-5-nitroaniline was added 42.1 g of methanesulfonyl chloride under ice-cooling, followed by stirring at room temperature for 7 hours. Water was added to the reaction solution, the precipitate was collected by filtration, and the crude crystals were recrystallized from ethanol to give 56.9 g of N-(2-fluoro-5-nitrophenyl)methanesulfonamide as pale yellow needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05521311 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-186308195b6b45559ca1ed03d6fd5297 |
| Source note | uspto-grants-1996_05 |