HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → benzyl (2R)-5-methoxy-2-methylpiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | benzyl (2R)-5-hydroxy-2-methylpiperidine-1-carboxylate | HCID 86724500 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | benzyl (2R)-5-methoxy-2-methylpiperidine-1-carboxylate | HCID 86724501 | — |
Reaction Steps
To a mixture of benzyl (2R)-5-hydroxy-2-methylpiperidine-1-carboxylate (368 mg, 1.47 mmol) dissolved in THF (4.9 mL) at 0° C. was added methyl iodide (0.32 mL, 5.08 mmol) followed by sodium hydride (78 mg, 3.25 mmol). The mixture was stirred for 2 hours at room temperature. The reaction was quenched with ice, and diluted with diethyl ether. The organic layer was washed with water and brine, dried over sodium sulfate, filtered and concentrated under reduced pressure to afford benzyl (2R)-5-methoxy-2-methylpiperidine-1-carboxylate. MS ESI calc'd. for C15H21NO3 [M+H]+ 264. found 264.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846657B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-374abcd4435e45fb8e8e928c9c3a2988 |
| Source note | uspto-grants-2014_09 |