HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → benzyl (2S,4R)-2-(fluoromethyl)-4-methoxypyrrolidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 57364082 | HCID 57364082 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | benzyl (2S,4R)-2-(fluoromethyl)-4-methoxypyrrolidine-1-carboxylate | HCID 86724496 | — |
Reaction Steps
To a solution of benzyl (2S,4R)-2-(fluoromethyl)-4-hydroxypyrrolidine-1-carboxylate (500 mg, 1.97 mmol) in THF (6.6 mL) at 0° C. was added methyl iodide (0.43 mL, 3.44 mmol) followed by sodium hydride (104 mg, 4.34 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 (2S,4R)-2-(fluoromethyl)-4-methoxypyrrolidine-1-carboxylate. MS ESI calc'd. for C14H18FNO3 [M+H]+ 268. found 268.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846657B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-e63ec6a922ea44958d4e06221a54b723 |
| Source note | uspto-grants-2014_09 |