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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752023Generated: October 28, 2026

Potassium Carbonate → HCID 67367623, compound

https://huagongshe.com/reaction/1752023

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 numberUS09162982B2
Source datasetuspto-grants-2015_10
ORD IDord-4259a3fbd2294919bbe6687c53a8187f
Source noteuspto-grants-2015_10