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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335257Generated: October 29, 2026

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

https://huagongshe.com/reaction/335257

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 numberUS08883828B2
Source datasetuspto-grants-2014_11
ORD IDord-58e7c07da2244c68a3695f2048a78bbe
Source noteuspto-grants-2014_11