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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887377Generated: October 26, 2026

Benzyl Bromide → 1-benzyl-N-methoxy-N-methylpiperidine-4-carboxamide

https://huagongshe.com/reaction/887377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantN-methoxy-N-methylpiperidine-4-carboxamideHCID 22405751—
SolventAcetoneHCID 180—
Product1-benzyl-N-methoxy-N-methylpiperidine-4-carboxamideHCID 21193030—

Reaction Conditions

Temperature80 °C

Reaction Steps

To the solution of N-methoxy-N-methylpiperidine-4-carboxamide (40 g, 232 mmol) in acetone (400 mL) was added benzyl bromide (42 mL, 349 mmol) and K2CO3 (64 g, 465 mmol) and the reaction mixture was stirred at 80° C. under reflux for 16 h. After completion of the reaction, the reaction mixture was filtered and acetone was removed under reduced pressure. The residue was purified by silica gel column chromatography (eluting with 50% ethyl acetate in hexane) to afford 1-benzyl-N-methoxy-N-methylpiperidine-4-carboxamide product. [M+1]=263.15

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247418B2
Source datasetuspto-grants-2012_08
ORD IDord-0529aad091ef4422a40388a97b8e4b84
Source noteuspto-grants-2012_08