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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 354836Erstellt: 25. Oktober 2026

Iodine → 1-Benzyl-3-(3-trifluoromethyl-phenyl)-piperidine-3-ol

https://huagongshe.com/reaction/354836

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktBenzene, 1-bromo-3-(trifluoromethyl)-HCID 9817—
Edukt3-Piperidinone, 1-(phenylmethyl)-HCID 96650—
EduktMagnesiumHCID 5462224—
LösungsmittelDiethyl EtherHCID 3283—
Produkt1-Benzyl-3-(3-trifluoromethyl-phenyl)-piperidine-3-olHCID 20506415—

Reaktionsschritte

Under anhydrous conditions, to a mixture of 11 g. of magnesium in 15 ml. of ethyl ether an iodine crystal is added followed by the addition of a solution of 100 g. of m-bromotrifluoromethylbenzene in 300 ml. of ether over a two hour period. The resulting mixture is stirred for two hours at ambient temperature then cooled to 5° C. A solution of 70 g. of N-benzyl-3-piperidone in 300 ml. of ether is added at this temperature over one hour. After stirring for 15 minutes at 5° C. and one hour at 20°-25° C., the reaction mixture was poured onto 800 ml. of ice-water with stirring. The mixture is filtered, the organic layer extracted with 4×100 ml. of 1 N hydrochloric acid and once with brine. The aqueous phase is made alkaline by addition of triethylamine in the cold and the resulting mixture extracted with ethyl acetate. The combined extracts are washed with brine, dried (MgSO4) and evaporated to dryness. The crude product is purified by silica gel chromatography, eluting with cyclohexane/chloroform/triethylamine (85:10:5 by volume) to obtain the desired product as an orange colored solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04377581
Quelldatensatzuspto-grants-1983_03
ORD IDord-fc3d377e13f8459aa5ea310dbfecdd61
Quellennotizuspto-grants-1983_03