HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → N-Methyl-4-nitrobenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 4-Nitrobenzenesulfonyl chloride | HCID 7404 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-Methyl-4-nitrobenzenesulfonamide | HCID 232993 | 98.4% |
Reaction Steps
To a suspension of 4-nitrobenzenesulfonyl chloride (5 g, 22.56 mmol) in ether (250 ml), methylamine (5 ml, 40% aq. solution, 56.4 mmol) was added, and the mixture was stirred at room temperature. After 16 hr, the reaction mixture was concentrated to remove the solvent and the residue was resuspended in methylene chloride. After washing with 2N HCl and brine, the organic fractions were dried (MgSO4), filtered and concentrated to give N-methyl-4-nitrobenzenesulfonamide (4.8 g, 98%): mp (DSC) 109° C. Anal Calc'd. for C7H8N2O4S: C, 38.89; H, 3.73; N, 12.96. Found: C, 38.83; H, 3.72; N, 12.96.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06815460B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-2d4445e8007b4c8997d59c74d8efd1b9 |
| Source note | uspto-grants-2004_11 |