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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806183Generated: October 31, 2026

1-Boc-4-[(N-methoxy-N-methylcarbamoyl)methyl]piperidine → Tert-butyl 4-(2-oxopropyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1806183

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-4-[(N-methoxy-N-methylcarbamoyl)methyl]piperidineHCID 22928781—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(2-oxopropyl)piperidine-1-carboxylateHCID 1201716999.1%

Reaction Steps

Added dropwise 3.0 M methylmagnesium chloride in THF (8.63 mL, 25.9 mmol) to a solution of tert-butyl 4-(2-(methoxy(methyl)amino)-2-oxoethyl)piperidine-1-carboxylate (5.93 g, 20.7 mmol) in THF (100 mL) at 0° C. Warmed to ambient temperature and stirred for 90 minutes. Partitioned between ether and 2N HCl, washed the organic layer twice with water, brine, dried, and concentrated to afford the title compound (4.95 g, 99.1% yield) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354540B2
Source datasetuspto-grants-2013_01
ORD IDord-4b9f5d54ab234aae85caa55a30ecc721
Source noteuspto-grants-2013_01