HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → 4-Methoxy-N-methylbenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-Methoxy-N-methylbenzenesulfonamide | HCID 2497429 | 48% |
Reaction Steps
To a solution of 4-methoxybenzene-1-sulfonyl chloride (2.4 g, 12 mmol) in CHCl3 (20 mL) was added methanamine (5 mL, 40 mmol) in EtOH. The mixture was stirred at room temperature for 16 h. The mixture was concentrated under reduced pressure. The resulting solid was washed with H2O (5 mL), ether, and air-dried to give 4-methoxy-N-methylbenzenesulfonamide (1.12 g, 48% yield) as a white solid. MS (ESI positive ion) m/z: 202 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820665B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-8c91cdf3fb394a8ca5fffbe9726aa7d0 |
| Source note | uspto-grants-2010_10 |