HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Methyl iodide → N-(4-bromo-2-ethylphenyl)-N-methylmethanesulfonamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | N-(4-bromo-2-ethylphenyl)methanesulfonamide | HCID 6469152 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-(4-bromo-2-ethylphenyl)-N-methylmethanesulfonamide | HCID 58762333 | 71,8% |
Reaktionsschritte
Methyl iodide (1.6 g, 0.0256M) was added to a mixture of N-(4-bromo-2-ethylphenyl)methanesulfonamide (4.77 g, 0.0171M) and potassium carbonate (3.5 g, 0.0256M) in dimethylformamide (50 ml) at room temperature under an atmosphere of nitrogen. The reaction mixture was stirred for a further 24 hrs after which time it was partitioned between diethylether (100 ml) and water (100 ml). The aqueous was extracted further with diethyl ether (2×100 ml). The combined organics were dried over magnesium sulfate, filtered and the solvent concentrated in vacuuo to afford the title compound as a brown oil (3.6 g). 1H NMR (CDCl3): δ 1.12 (t, J=8.60 Hz, 3H), 2.94 (m, 5H), 3.02 (s, 3H), 6.71 (d, J=8.5 Hz, 1H), 7.05 (d, J=8.5 Hz, 1H), 7.28 (s, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07473790B2 |
| Quelldatensatz | uspto-grants-2009_01 |
| ORD ID | ord-697c9930f80c40378d9e2b3b6c013933 |
| Quellennotiz | uspto-grants-2009_01 |