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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2191918Generated: November 2, 2026

Ethyl Acetate → 1-(1-Benzylpiperidin-4-yl)ethanone

https://huagongshe.com/reaction/2191918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-benzyl-N-methoxy-N-methylpiperidine-4-carboxamideHCID 21193030—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
Product1-(1-Benzylpiperidin-4-yl)ethanoneHCID 910923—

Reaction Conditions

Temperature27.5 °C

Reaction Steps

To a stirred solution of 1-benzyl-N-methoxy-N-methylpiperidine-4-carboxamide (11.5 g, 44 mmol) in diethyl ether (150 mL) at 0° C. was added methyl magnesium bromide (15.7 g, 132 mmol), drop-wise over 10 min. The resulting mixture was stirred at 25-30° C. for 2 h. After completion of the reaction, the mixture was treated with EtOAc and saturated NH4Cl solution. The separated organic layer was washed with brine and dried over anhydrous sodium sulfate and concentrated under vacuum to afford 1-(1-benzylpiperidin-4-yl)ethanone product. [M+1]=218.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329700B2
Source datasetuspto-grants-2012_12
ORD IDord-ec427f758b47444bafc049ea09cbb313
Source noteuspto-grants-2012_12