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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012241Generated: October 27, 2026

Water → tert-butyl (R)-3-methoxymethylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1012241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactanttert-butyl (3R)-3-(hydroxymethyl)piperidine-1-carboxylateHCID 1514447—
SolventDimethylformamideHCID 6228—
Producttert-butyl (R)-3-methoxymethylpiperidine-1-carboxylateHCID 58826553105.6%

Reaction Steps

To a solution of tert-butyl (R)-3-hydroxymethylpiperidine-1-carboxylate (11.50 g, 53.7 mmol) in N,N-dimethylformamide (110 ml) was added sodium hydride (3.22 g, 80.6 mmol) under ice-cooling, and the mixture was stirred at room temperature for 20 min. To the reaction mixture was added methyl iodide (4.35 ml, 69.9 mmol) under ice-cooling, and the mixture was stirred at room temperature for 1 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to give tert-butyl (R)-3-methoxymethylpiperidine-1-carboxylate (13.00 g, yield 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977331B1
Source datasetuspto-grants-2011_07
ORD IDord-fa25481f88784feda7f968545fdab1df
Source noteuspto-grants-2011_07