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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 71206Generated: October 28, 2026

Hydrochloric Acid → 1-(4-Methoxybenzyl)-3-(3,4,5-trifluorophenoxy)piperidin-2-one

https://huagongshe.com/reaction/71206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 1-(4-methoxybenzyl)-2-oxo-3-(3,4,5-trifluorophenoxy)piperidine-3-carboxylateHCID 66607388—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Methoxybenzyl)-3-(3,4,5-trifluorophenoxy)piperidin-2-oneHCID 6660813385.7%

Reaction Steps

A mixture of ethyl 1-(4-methoxybenzyl)-2-oxo-3-(3,4,5-trifluorophenoxy)piperidine-3-carboxylate (352 mg) and 1N aqueous sodium hydroxide solution (1.6 mL) in THF (3 mL) was stirred at room temperature for 2 days, and acidified with 1N hydrochloric acid, and extracted with ethyl acetate. The organic layer was separated, washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was recrystallized from ethyl acetate/hexane, the white crystals were separated by filtration, and the filtrate was concentrated. A mixture of the residue and the white crystals in toluene (3 mL) was stirred at 100° C. for 1 hr, and the solvent was evaporated under reduced pressure to give the title compound (252 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822699B2
Source datasetuspto-grants-2014_09
ORD IDord-2ca7903418af4c3a859603f1cb70c681
Source noteuspto-grants-2014_09