Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465709Generated: October 31, 2026

Tert-butyl 3-[methoxy(methyl)carbamoyl]piperidine-1-carboxylate → tert-Butyl 3-acetylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1465709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-[methoxy(methyl)carbamoyl]piperidine-1-carboxylateHCID 22248320—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 3-acetylpiperidine-1-carboxylateHCID 2526000270.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Tert-butyl 3-(methoxy(methyl)carbamoyl)piperidine-1-carboxylate (8.17 g, 30 mmol) was dissolved in THF (100 mL) and cooled to 0° C., methylmagnesium bromide (3.0 M in Et2O, 11 mL, 33 mmol) was added dropwise. The reaction mixture was warmed to room temperature and stirred overnight. After quench with saturated NH4Cl, the reaction mixture was extracted with EtOAc, dried and concentrated. The crude product was column purified with mixture of hexane and EtOAc to give tert-butyl 3-acetylpiperidine-1-carboxylate (4.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999966B2
Source datasetuspto-grants-2015_04
ORD IDord-6c45a7c41d2a49748a83d3c5b41057ae
Source noteuspto-grants-2015_04