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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1031545Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1031545

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktHexafluorobenzeneHCID 9805—
EduktSodium hydrideHCID 24758—
Edukt4-Phenylpiperidin-4-olHCID 96387—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(2,3,4,5,6-Pentafluorophenoxy)-4-phenylpiperidineHCID 1464997844%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04954511
Quelldatensatzuspto-grants-1990_09
ORD IDord-328e9c6847e348d78475cd9183d1ee0d
Quellennotizuspto-grants-1990_09