HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 5-(4-Bromophenyl)-1-methyl-2-pyrrolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-(4-BROMOPHENYL)PYRROLIDIN-2-ONE | HCID 12056595 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(4-Bromophenyl)-1-methyl-2-pyrrolidinone | HCID 57762794 | 67% |
Reaction Steps
A solution of 5-(4-bromophenyl)-2-pyrrolidinone (preparation described in WO00/21958) (200 mg, 0.83 mmol) in dimethylformamide (5 ml) was treated with a solid suspension of sodium hydride (60% in mineral oil, 35 mg, 0.88 mmol). The reaction mix was allowed to stir for 20 minutes, then methyl iodide (124 mg, 0.88 mmol) was added and the whole mix stirred for a further 18 hours. The reaction mixture was quenched with a few drops of water then partitioned between dichloromethane (15 ml), and water (60 ml), the organic layer was removed and washed with water again (2×10 ml), then reduced to minimum volume under reduced pressure to give the title compound as a brown oil (141 mg, 67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07642256B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-17a48ccbeb7e423cb586a60b37a37227 |
| Source note | uspto-grants-2010_01 |