HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Benzyl 4-methoxy-2-(1-methoxycyclopropyl)pyrrolidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzyl 2-(1-hydroxycyclopropyl)-4-methoxypyrrolidine-1-carboxylate | HCID 86724493 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzyl 4-methoxy-2-(1-methoxycyclopropyl)pyrrolidine-1-carboxylate | HCID 86724494 | — |
Reaction Steps
To a mixture of benzyl 2-(1-hydroxycyclopropyl)-4-methoxypyrrolidine-1-carboxylate (312 mg, 1.07 mmol) dissolved in THF (3.6 mL) at 0° C. was added methyl iodide (0.23 mL, 3.68 mmol) followed by sodium hydride (56.5 mg, 2.36 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. The residue was purified by silica gel chromatography (0-20% methanol/dichloromethane, linear gradient) to afford benzyl 4-methoxy-2-(1-methoxycyclopropyl)pyrrolidine-1-carboxylate. MS ESI calc'd. for C17H23NO4 [M+H]+ 306. found 306.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846657B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-6f9abe76738a409d8b16bec992f79f2c |
| Source note | uspto-grants-2014_09 |