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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398200Generated: October 25, 2026

Water → Ethyl 2-oxo-3-(3,4,5-trifluorophenoxy)piperidine-3-carboxylate

https://huagongshe.com/reaction/1398200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-chloro-2-oxopiperidine-3-carboxylateHCID 568505—
Reactant3,4,5-TrifluorophenolHCID 2777943—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductEthyl 2-oxo-3-(3,4,5-trifluorophenoxy)piperidine-3-carboxylateHCID 6660765979.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 3,4,5-trifluorophenol (14.4 g) and potassium carbonate (40.3 g) in DMF (200 mL) was added ethyl 3-chloro-2-oxopiperidine-3-carboxylate (20 g), and the mixture was stirred at 100° C. for 1 hr. To the reaction mixture were added water (200 mL) and saturated brine (200 mL) at 0° C., and the mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogen carbonate solution (200 mL), water (200 mL) and saturated brine (200 mL×2), and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (24.61 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901309B2
Source datasetuspto-grants-2014_12
ORD IDord-0b49089dede144028afeff197bbed87b
Source noteuspto-grants-2014_12