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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217433Generated: October 29, 2026

Water → Methyl 4-piperidin-1-yl-2-(trifluoromethyl)benzoate

https://huagongshe.com/reaction/217433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPiperidineHCID 8082—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-fluoro-2-(trifluoromethyl)benzoateHCID 15541084—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-piperidin-1-yl-2-(trifluoromethyl)benzoateHCID 58439025—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of methyl 4-fluoro-2-(trifluoromethyl)benzoate in DMF were added K2CO3 and piperidine, followed by stirring at 100° C. for 3 hours. The reaction mixture was cooled to 0° C., and water was added thereto, followed by extraction with EtOAc. The organic layer was washed with brine, dried over MgSO4, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:EtOAc=100:0 to 90:10) to obtain methyl 4-piperidin-1-yl-2-(trifluoromethyl)benzoate as a colorless oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193378B2
Source datasetuspto-grants-2012_06
ORD IDord-caf402de862249dbac773b2155761377
Source noteuspto-grants-2012_06