HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-Methyl-N-(2-nitrophenyl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(2-nitrophenyl)methanesulfonamide | HCID 296454 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-Methyl-N-(2-nitrophenyl)methanesulfonamide | HCID 13314625 | 38% |
Reaction Steps
To a cooled (0° C.) solution of N-(2-nitrophenyl)methanesulfonamide (50 mg, 0.231 mmol) in DMF (2 mL) was added sodium hydride (11 mg, 0.46 mmol) and the reaction was warmed to room temperature and stirred for 20 minutes. The reaction was then re-cooled to 0° C. and iodomethane (0.029 mL 0.46 mmol) was added. The reaction was warmed to room temperature and stirred for 3 hours. The crude reaction was concentrated and purified by silica gel chromatography to provide N-methyl-N-(2-nitrophenyl)methanesulfonamide (20 mg, 38% yield). 1H NMR (300 MHz, CDCl3) δ 7.91 (m, 1H), 7.70-7.50 (m, 3H), 3.34 (s, 3H), 3.01 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09315494B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-0a0c419b87e24a608182d6b306ff999a |
| Source note | uspto-grants-2016_04 |