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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 66675Erstellt: 23. Oktober 2026

Water → (4-Bromophenyl)-(1-methyl-4-piperidinyl)methanone

https://huagongshe.com/de/reaction/66675

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktBenzonitrile, 4-bromo-HCID 12162—
EduktAmmonium ChlorideHCID 25517—
Edukt4-chloro-N-methylpiperidineHCID 79342—
EduktMagnesiumHCID 5462224—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(4-Bromophenyl)-(1-methyl-4-piperidinyl)methanoneHCID 20530733—

Reaktionsschritte

To a stirred and cooled (10°-15° C.) Grignard-complex, previously prepared starting from 13.5 parts of 4-chloro-1-methylpiperidine and 2.4 parts of magnesium in 68 parts of tetrahydrofuran, is added dropwise a solution of 10 parts of 4-bromobenzonitrile in 22 parts of tetrahydrofuran. Upon completion, stirring is continued for 1 hour at reflux temperature. The reaction mixture is decomposed by pouring onto a mixture of 50 parts of ammonium chloride in 250 parts of water. The product is extracted with methylbenzene. The extract is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions are collected and the eluent is evaporated, yielding 10 parts of (4-bromophenyl)-(1-methyl-4-piperidinyl)methanone as a residue.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04342870
Quelldatensatzuspto-grants-1982_08
ORD IDord-93eec3e9667745f9b5688539be76b279
Quellennotizuspto-grants-1982_08