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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915914Generated: October 27, 2026

Methyl iodide → Benzyl 4-methoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/915914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantBenzyl 4-Hydroxy-1-piperidinecarboxylateHCID 2794620—
SolventEthyl AcetateHCID 8857—
ProductBenzyl 4-methoxypiperidine-1-carboxylateHCID 2302430194%

Reaction Steps

To a 20 ml tetrahydrofuran solution of 1.87 g (7.95 mmol) of benzyl 4-hydroxy-1-piperidinecarboxylate, 413 mg (60% in oil, 10.33 mmol) of sodium hydride and 792 μl (12.72 mmol) of methyl iodide were added at 0° C., and the mixture was stirred at room temperature for 16.5 hours. Then, the reaction mixture was diluted with ethyl acetate, and washed with water. The washed system was dried over sodium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=2/1) to obtain 2.08 g (94%) of the captioned compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268128B2
Source datasetuspto-grants-2007_09
ORD IDord-3faf55943fe7472bbbcdb55c630b4593
Source noteuspto-grants-2007_09