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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1792507Erstellt: 25. Oktober 2026

Water → t-Butyl 4-(4-trifluoromethylsulfonylphenoxy)piperidine-1-carboxylate

https://huagongshe.com/reaction/1792507

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium BicarbonateHCID 516892—
Eduktt-Butyl 4-(4-trifluoromethylsulfanyl-phenoxy)piperidine-1-carboxylateHCID 22031376—
EduktSodium periodateHCID 23667635—
KatalysatorRuthenium trichloride hydrateHCID 6093376—
Produktt-Butyl 4-(4-trifluoromethylsulfonylphenoxy)piperidine-1-carboxylateHCID 22031673—

Reaktionsschritte

2.55 g sodium periodate and 0.4 mg ruthenium (III) chloride hydrate were added to 60 mL solution mixture (carbon tetrachloride/acetonitrile/water=1:1:2) of 1.5 g t-butyl 4-(4-trifluoromethylsulfanyl-phenoxy)piperidine-1-carboxylate (compound in Production Example 454) with stirring under ice-cooling, and the mixture was stirred at room temperature for 1 hour. Water and a sodium bicarbonate solution were added thereto, and the reaction solution was extracted with ethyl acetate, dried over sodium sulfate and purified by silica gel chromatography (hexane/ethyl acetate) to give 1.3 g t-butyl 4-(4-trifluoromethylsulfonylphenoxy)piperidine-1-carboxylate. 2 mL solution of 4 N hydrogen chloride in ethyl acetate was added thereto and left for 1 hour. The solvent was removed, and the precipitated crystals were washed with ethyl acetate/ether to give 965 mg of the title compound as colorless crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07074801B1
Quelldatensatzuspto-grants-2006_07
ORD IDord-7db1e17f438440e89fa606a0b0807925
Quellennotizuspto-grants-2006_07