Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1248202Erstellt: 25. Oktober 2026

Water → (1-Benzylpiperidin-4-yl)(2-methylphenyl)methanone

https://huagongshe.com/reaction/1248202

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt2-BromotolueneHCID 7236—
EduktAmmonium ChlorideHCID 25517—
Edukt1-Benzylpiperidine-4-carbonitrileHCID 793383—
EduktMagnesiumHCID 5462224—
LösungsmittelDiethyl EtherHCID 3283—
Produkt(1-Benzylpiperidin-4-yl)(2-methylphenyl)methanoneHCID 20530712—

Reaktionsbedingungen

Temperatur10 °C

Reaktionsschritte

To 7 parts of magnesium is added dropwise a solution of 50 parts of 1-bromo-2-methylbenzene in 140 parts of 1,1'-oxybisethane so that the mixture is refluxing. The whole is stirred for 15 minutes at reflux. The Grignard-complex is cooled to 10° C. and there is added dropwise a solution of 30 parts of 1-(phenylmethyl)-4-piperidinecarbonitrile in 70 parts of 1,1'-oxybisethane. Upon completion, stirring is continued for 4 hours at room temperature. The reaction mixture is decomposed with a solution of 40 parts of ammonium chloride in 400 parts of water. The organic phase is separated, dried, filtered and evaporated, yielding 31 parts of (2-methylphenyl) [1-(phenylmethyl)-4-piperidinyl]methanone as an oily residue.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04522945
Quelldatensatzuspto-grants-1985_06
ORD IDord-53d87a40c9db4df29be11c9aaca6526c
Quellennotizuspto-grants-1985_06