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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887378Generated: October 30, 2026

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

https://huagongshe.com/reaction/887378

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 numberUS08247418B2
Source datasetuspto-grants-2012_08
ORD IDord-f2d4fe5c3c7f4c04977529d2f4e1cfcc
Source noteuspto-grants-2012_08