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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81147Generated: October 30, 2026

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

https://huagongshe.com/reaction/81147

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 C15H21NO3 [M+H]+ 264. found 264.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846657B2
Source datasetuspto-grants-2014_09
ORD IDord-374abcd4435e45fb8e8e928c9c3a2988
Source noteuspto-grants-2014_09