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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809550Generated: October 31, 2026

1-acetyl-N-methoxy-N-methylpiperidine-4-carboxamide → 1,4-Diacetylpiperidine

https://huagongshe.com/reaction/1809550

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-acetyl-N-methoxy-N-methylpiperidine-4-carboxamideHCID 18713548—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product1,4-DiacetylpiperidineHCID 277725082.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 1000 mL flask, 1-acetyl-N-methoxy-N-methylpiperidine-4-carboxamide (59.10 g, 276 mmol) was dissolved in THF (800 mL) and cooled to 0° C. Methylmagnesium bromide (110.3 mL, 331 mmol) (3.0M in diethyl ether) was added slowly and the resulting white slurry was agitated for 1 hour. The reaction was quenched with 300 mL of 2M HCl and the solvent was evaporated. The resulting aqueous slurry was filtered and the solids were washed with water and small amount of ether to provide the title compound (38.4 g, 82.2% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362037B2
Source datasetuspto-grants-2013_01
ORD IDord-0fcce69ff88842eabc084af85ccd5475
Source noteuspto-grants-2013_01