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HRID 1031547Erstellt: 26. Oktober 2026

Water → 4-(4-Methylphenyl)-1-methyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidine

https://huagongshe.com/reaction/1031547

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktHexafluorobenzeneHCID 9805—
EduktSodium hydrideHCID 24758—
Edukt1-Methyl-4-(4-methylphenyl)piperidin-4-OLHCID 14837037—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(4-Methylphenyl)-1-methyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidineHCID 14837063—

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

To a suspension of sodium hydride (2.2 g, 60% in oil) in 20 ml of dimethylformamide, was added a solution of 11.0 g of 4-hydroxy-4-(4-methylphenyl)-1-methylpiperidine in 50 ml of dimethylformamide. After heating to 85° C. for thirty minutes, the mixture was cooled with an ice-bath, and treated over a period of ten minutes with a solution of 7 ml of hexafluorobenzene in 20 ml of dimethylformamide. After stirring at ambient temperature for twenty hours, the mixture was poured into 200 ml water, stirred for five minutes, then extracted with ethyl acetate (2×). The organic layer was washed with water (2×), followed by a saturated solution of sodium chloride, and dried over anhydrous magnesium sulfate. After filtering, evaporation of the solvent afforded a residue which was purified by means of high pressure liquid chromatography (silica gel; elution with 10% methanol/dichloromethane). The desired fractions were combined, and evaporated to yield 13 g of (4-(4-methylphenyl)-1-methyl-4-(2,3,4,5,6-pentafluorophenoxy)piperidine as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04954511
Quelldatensatzuspto-grants-1990_09
ORD IDord-9e892695c03d40eab71f96993ded0761
Quellennotizuspto-grants-1990_09