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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 467064Erstellt: 24. Oktober 2026

Ethanol → (-)-trans-1(2-Cyanoethyl)-4-(4-fluorophenyl)-3-(3,4-methylenedioxyphenoxymethyl)-piperidine hydrochloride

https://huagongshe.com/de/reaction/467064

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktPotassium CarbonateHCID 11430—
Edukt3-BromopropionitrileHCID 17020—
EduktParoxetine HydrochlorideHCID 62878—
LösungsmittelAcetoneHCID 180—
LösungsmittelDiethyl EtherHCID 3283—
Produkt(-)-trans-1(2-Cyanoethyl)-4-(4-fluorophenyl)-3-(3,4-methylenedioxyphenoxymethyl)-piperidine hydrochlorideHCID 67638429—

Reaktionsschritte

1 g of (-)-trans-4-(4-fluorophenyl)-3-(3,4-methylene dioxyphenoxymethyl)-piperidine hydrochloride in 50 ml 99 9% ethanol was mixed with 3-bromopropionitrile (7 ml) and 2 g potassium carbonate. The mixture was refluxed for 70 h. After cooling 25 ml acetone and 25 ml diethylether were added, the precipitate filtered off, and the filtrate evaporated in vacuo. The residue was extracted with 1N NaOH/ether, the ether layer dried (MgSO4) and evaporated to dryness. The residue was dissolved in acetone and excess conc. HCl was added. Subsequent evaporation gave a hard glass, which was purified on a silica gel column using 99.5% ethanol as eluent. The title compound was isolated, and its structure confirmed by the IR and NMR data. M.p. 156° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05158961
Quelldatensatzuspto-grants-1992_10
ORD IDord-eb66a0f4ae404633a525c7dfed23e0e5
Quellennotizuspto-grants-1992_10