HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-[(4-bromophenyl)methyl]-N-methyl-1-pyrrolidinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-[(4-bromophenyl)methyl]-1-pyrrolidinecarboxamide | HCID 57762826 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[(4-bromophenyl)methyl]-N-methyl-1-pyrrolidinecarboxamide | HCID 57762825 | 103.9% |
Reaction Steps
N-[(4-bromophenyl)methyl]-1-pyrrolidinecarboxamide (230 mg, 0.81 mmol), was dissolved in dimethylformamide (2 ml) and treated at room temperature with a 60% sodium hydride suspension in mineral oil (33 mg, 0.83 mmol). This mix was stirred for 15 minutes before being treated with iodomethane (116 mg, 0.82 mmol). The resulting mix was stirred at 20° C. for a total of 16.5 hours. The reaction was quenched with water (4 ml) and extracted into ethyl acetate (4 ml). The organic layer was dried over sodium sulphate and the solvent removed under reduced pressure to give the title compound as a colourless oil (250 mg, crude). LC/Mass Spec (ES): Found 297 (ES+), retention time 2.90 mins. C13H1779BrN2O requires 296.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07642256B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-bf365dfa748642e69fc5ca3488b64d76 |
| Source note | uspto-grants-2010_01 |