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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389647Generated: October 31, 2026

Methyl iodide → (R)-tert-Butyl 3-methoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/389647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant(R)-1-Boc-3-hydroxypiperidineHCID 1514398—
SolventDimethylformamideHCID 6228—
Product(R)-tert-Butyl 3-methoxypiperidine-1-carboxylateHCID 67155503—

Reaction Steps

To commercially available (R)-3-hydroxy-piperidine-1-carboxylic acid tert-butyl ester (4.5 g, 22.36 mmol) in 60 ml DMF at 0° C. was added NaH (1.3 g, 33.54 mmol, 55-65 in mineral oil) under stirring in three portions under an argon atmosphere. After 20 min methyl iodide (4.76 g, 33.54 mmol) was added and the reaction was warmed to RT and stirred for another 3 h. After quenching with sat. aq NaHCO3-solution the mixture was extracted with ethyl acetate. The organic layer was washed with 1N KHSO4 and brine. The organic layer was dried with MgSO4, filtered and evaporated. The crude material was purified by chromatography on silica gel. Yield: 4.6 g, 96

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378092B2
Source datasetuspto-grants-2013_02
ORD IDord-77ab5b10d8f7401294e939460bbe276e
Source noteuspto-grants-2013_02