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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852755Generated: November 1, 2026

Methyl iodide → benzyl (2R)-5-methoxy-2-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1852755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactantbenzyl (2R)-5-hydroxy-2-methylpiperidine-1-carboxylateHCID 86724500—
SolventTetrahydrofuranHCID 8028—
Productbenzyl (2R)-5-methoxy-2-methylpiperidine-1-carboxylateHCID 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 C16H21NO3 [M+H]+ 264. found 264.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962611B2
Source datasetuspto-grants-2015_02
ORD IDord-e4be3a38929d43daaa15f77eec3002de
Source noteuspto-grants-2015_02