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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 444338Erstellt: 24. Oktober 2026

Ammonium Chloride → 1-Benzyl-3-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]3-hydroxypiperidine

https://huagongshe.com/de/reaction/444338

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt3-Piperidinone, 1-(phenylmethyl)-HCID 96650—
EduktMagnesiumHCID 5462224—
Edukt2-(Benzyloxy)-1-bromo-4-(2-methyloctan-2-YL)benzeneHCID 12882164—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Benzyl-3-[2-benzyloxy-4-(1,1-dimethylheptyl)phenyl]3-hydroxypiperidineHCID 1557155667%

Reaktionsbedingungen

Temperatur-10 °C

Reaktionsschritte

A solution of 20.0 g. (51.4 mmols) of 1-bromo-2-benzyloxy-4-(1,1-dimethylheptyl)benzene in 75 ml. of tetrahydrofuran is slowly added to 2.5 g. (103 mmols) of 70-80 mesh magnesium metal. The resulting mixture is refluxed for 20 minutes and is then cooled to -10° C. A solution of 9.71 g. (51.4 mmols) of N-benzyl-3-piperidone in 25 ml. of tetrahydrofuran is then added at such a rate that the reaction temperature is maintained below 0° C. The reaction mixture is stirred for 30 minutes following completion of addition and is then added to 500 ml. of saturated ammonium chloride and 500 ml. of ether. The ether extract is washed with two 250 ml. portions of sodium chloride, dried over magnesium sulfate and evaporated to an oil. The oil is purified via column chromatography on 700 g. of silica gel eluted with 50% ether-cyclohexane to yield 17.1 g. (67%) of the title compound as an oil:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04263438
Quelldatensatzuspto-grants-1981_04
ORD IDord-69b01e05c9334009aad76f328f777b90
Quellennotizuspto-grants-1981_04