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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911933Generated: October 30, 2026

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

https://huagongshe.com/reaction/911933

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 numberUS08022223B2
Source datasetuspto-grants-2011_09
ORD IDord-a5cbaa1e64124c1fa7c53e71dc986c62
Source noteuspto-grants-2011_09