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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 484733Erstellt: 24. Oktober 2026

Ammonium Chloride → alpha-(2-Fluorophenyl)-1-methyl-alpha-phenyl-4-piperidinemethanol

https://huagongshe.com/de/reaction/484733

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt2-FluorobenzophenoneHCID 67650—
Edukt4-chloro-N-methylpiperidineHCID 79342—
EduktMagnesiumHCID 5462224—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produktalpha-(2-Fluorophenyl)-1-methyl-alpha-phenyl-4-piperidinemethanolHCID 2332606544%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirred and refluxing Grignard complex previously prepared starting from 80.2 parts of 4-chloro-1-methylpiperidine, 14.6 parts of magnesium and 270 parts of tetrahydrofuran, was added dropwise a solution of 101 parts of (2-fluorophenyl)phenylmethanone in 450 parts of tetrahydrofuran. Upon completion, stirring was continued for 18 hours at reflux temperature. The reaction mixture was cooled in an ice-bath and decomposed with a solution of 32 parts of ammonium chloride in 160 parts of water. After stirring for 30 minutes, the product was filtered off and washed with tetrahydrofuran. The filtrate was evaporated, the residue was taken up in methylbenzene and the latter was evaporated again in a boiling water-bath. The residue was dissolved in 700 parts of 2,2'-oxybispropane. The turbid solution was filtered and gaseous hydrogen chloride was bubbled through the filtrate. The solid product was filtered off and suspended in 1000 parts of water. The suspension was treated with ammonium hydroxide and extracted twice with 280 parts of 1,1'-oxybisethane. The combined extracts were dried, filtered and evaporated. The oily residue was crystallized from 240 parts of acetonitrile. After cooling to 0° C., the product was filtered off and dried, yielding 66 parts (44%) of α-(2-fluorophenyl)-1-methyl-α-phenyl-4-piperidinemethanol (intermediate 33).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04533665
Quelldatensatzuspto-grants-1985_08
ORD IDord-9191ce33cb1945b78c98a3f325d17c35
Quellennotizuspto-grants-1985_08