HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-(4-Methoxy-2-methyl-phenyl)-N-methyl-methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-(4-methoxy-2-methylphenyl)methanesulfonamide | HCID 15851883 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(4-Methoxy-2-methyl-phenyl)-N-methyl-methanesulfonamide | HCID 21931865 | — |
Reaction Steps
To a solution of 860 mg (4.0 mmol) N-(4-methoxy-2-methyl-phenyl)-methanesulfonamide in 15 ml DMF at ambient temperature was added 192 mg (48 mmol) 60% sodium hydride dispersion and the resulting mixture was treated with 1.14 gm, 0.5 ml (8.0 mmol) methyl iodide. The reaction mixture was stirred at room temperature for 2 hours and 0.5 ml of methyl iodide was introduced and the reaction mixture was stirred at room temperature for 16 hours. The reaction mixture was diluted with 1N HCl and then extracted with ethyl acetate. The organics were washed with brine, dried with sodium sulfate and then evaporated in vacuo to afford 293 mg (X %) of a light purple solid. Mass spectrum APCI (m/z) 230 (p+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07119207B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-d8150dc647fd4e398604cdb269f3f0a1 |
| Source note | uspto-grants-2006_10 |