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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806155Generated: October 30, 2026

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

https://huagongshe.com/reaction/1806155

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

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 numberUS08354540B2
Source datasetuspto-grants-2013_01
ORD IDord-49559709607047b2b0f85d8efdac682f
Source noteuspto-grants-2013_01