HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → 5-fluoro-N-methyl-2-nitrobenzene-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 5-Fluoro-2-nitrobenzene-1-sulfonyl chloride | HCID 12904368 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-fluoro-N-methyl-2-nitrobenzene-1-sulfonamide | HCID 67114956 | — |
Reaction Steps
A solution of 5-fluoro-2-nitrobenzene-1-sulfonyl chloride (2.0 g, 8.35 mmol) in dichloromethane (50 mL) was cooled using an ice water bath. 2M methylamine in tetrahydrofuran (5.0 mL, 10.0 mmol) was added. The resulting solution was stirred for 2 hours. The reaction mixture was washed with 2N HCl solution (2×100 mL), brine (100 mL) and then dried over magnesium sulphate. The solution was filtered before concentrating under reduced pressure to afford 5-fluoro-N-methyl-2-nitrobenzenesulfonamide (1.79 g, 7.64 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08841289B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-78d01554a28249009d4852ceca6c6663 |
| Source note | uspto-grants-2014_09 |