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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887692Generated: October 30, 2026

Potassium Carbonate → HCID 67367623, compound

https://huagongshe.com/reaction/887692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,4,6-TrifluorophenolHCID 519974—
Reactant4-(2-Methanesulfonyloxymethylphenyl)piperidine-1-carboxylic Acid t-Butyl EsterHCID 46213046—
SolventAcetonitrileHCID 6342—
ProductHCID 67367623HCID 6736762386.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

4-(2-Methanesulfonyloxymethylphenyl)piperidine-1-carboxylic acid t-butyl ester (27.0 g, 60.6 mmol, 1.0 eq.) was dissolved in MeCN (540 mL) and added to K2CO3 (25 g, 180 mmol, 3.0 eq.) and 2,4,6-trifluorophenol (13.5 g, 90.9 mmol, 1.5 eq.). The mixture was vigorously stirred at 50° C. for 6 hours, removed from the heat, and stirred overnight. The mixture was cooled at room temperature, and diluted with EtOAc (700 mL) and water (700 mL). The phases were separated, and the organic layer was washed twice with 1.0 M NaOH in water (2×400 mL) and saturated aqueous NaCl (1×400 mL), then dried over Na2SO4 and the solvent removed to yield crude 4-[2-(2,4,6-trifluorophenoxymethyl)phenyl]piperidine-1-carboxylic acid t-butyl ester (25.0 g). The crude product was combined with smaller scale runs for a total of 30 g, and purified by chromatography (0-10% EtOAc in hexanes) to yield 4-[2-(2,4,6-trifluorophenoxymethyl)phenyl]piperidine-1-carboxylic acid t-butyl ester (22.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247433B2
Source datasetuspto-grants-2012_08
ORD IDord-3b0b7804889f4d7bb724cb78890dc750
Source noteuspto-grants-2012_08