HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 21964391, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 21964343 | HCID 21964343 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21964391 | HCID 21964391 | — |
Reaction Steps
A solution of 1-benzyl-3-(3-chlorophenyl)-4-piperidone (75 mmol) in anhydrous THF (250 mL) is cooled to −30° C., then treated with a solution of freshly prepared lithium diisopropylamide (2.0 M in THF/heptane, 45 mL). After stirring for 15 min, a solution of methyl iodide (80 mmol) in THF (40 mL) is rapidly added. The mixture is then stirred for 1 hour at −30° C., warmed quickly to room temperature, and quenched with a saturated aqueous solution of ammonium chloride. The organic layer is collected, washed with water, brine, and dried (MgSO4). After filtering, the filtrate is concentrated in vacuo to afford the desired intermediate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07449490B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-76df91655ec24c6f9bf748ea61ac8447 |
| Source note | uspto-grants-2008_11 |