HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1-(4-Bromo-2-(methoxymethyl)phenyl)-2-ethylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (5-Bromo-2-(2-ethylpiperidin-1-YL)phenyl)methanol | HCID 58554150 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-Bromo-2-(methoxymethyl)phenyl)-2-ethylpiperidine | HCID 58554165 | 97% |
Reaction Steps
To a solution of sodium hydride (2.3 g, 93 mmol) in anhydrous DMF (130 mL) was added a solution of [5-bromo-2-(2-ethylpiperidin-1-yl)phenyl]methanol (15 g, 48.3 mmol) in DMF (20 mL) drop wise at 0° C. After 30 minutes, methyl iodide was added drop wise at 0° C. The reaction mixture was quenched with a saturated aqueous solution of NH4Cl (30 mL), then diluted with water (100 mL) and extracted with EtOAc. The organic layer was dried (Na2SO4) and concentrated under reduced pressure to afford the title compound as a yellow oil (15.2 g, 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08815919B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-9e170b145cb34fb2a8ca56beb396a752 |
| Source note | uspto-grants-2014_08 |