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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1031545Generated: October 23, 2026

Water → 4-(2,3,4,5,6-Pentafluorophenoxy)-4-phenylpiperidine

https://huagongshe.com/en/reaction/1031545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHexafluorobenzeneHCID 9805—
ReactantSodium hydrideHCID 24758—
Reactant4-Phenylpiperidin-4-olHCID 96387—
SolventDimethylformamideHCID 6228—
Product4-(2,3,4,5,6-Pentafluorophenoxy)-4-phenylpiperidineHCID 1464997844%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a suspension of sodium hydride (60% in oil, 6.4 g) in 50 ml of dry dimethylformamide was added, over a period of ten minutes, a solution of 25 g of 4-hydroxy-4-phenylpiperidine in 100 ml of dry dimethylformamide. After stirring at 50° C., for thirty minutes, the reaction mixture was cooled to ice bath temperature (5° C.). A solution of 18.6 ml of hexafluorobenzene in 100 ml of dry dimethylformamide was then added over a period of thirty minutes, and the resulting mixture stirred at ambient temperature for twenty hours. The mixture was poured into 500 ml water, stirred for five minutes, and extracted with ethyl acetate. The organic layer was washed with water followed by a saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After filtering, evaporation of the solvents afforded a residue which was purified by means of high pressure liquid chromatography (silica gel; elution with 20% methanol/dichloromethane) to afford 21 g (44%) of 4-(2,3,4,5,6-pentafluorophenoxy)-4-phenylpiperidine as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04954511
Source datasetuspto-grants-1990_09
ORD IDord-328e9c6847e348d78475cd9183d1ee0d
Source noteuspto-grants-1990_09