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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 66673Erstellt: 23. Oktober 2026

Iodine → (3-Methylphenyl) (1-methyl-4-piperidinyl)methanone

https://huagongshe.com/de/reaction/66673

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktWaterHCID 962—
Edukt1,2-DibromoethaneHCID 7839—
Edukt3-TolunitrileHCID 12104—
EduktAmmonium ChlorideHCID 25517—
Edukt4-chloro-N-methylpiperidineHCID 79342—
EduktMagnesiumHCID 5462224—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(3-Methylphenyl) (1-methyl-4-piperidinyl)methanoneHCID 12852040—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

To 5 parts of magnesium are added 2.18 parts of 1,2-dibromoethane and a small amount of iodine to initiate the reaction. Then there is added dropwise a solution of 28 parts of 4-chloro-1-methylpiperidine in 180 parts of tetrahydrofuran while the mixture is heated to 70° C. After cooling, there is added dropwise a solution of 14 parts of 3-methylbenzonitrile in 90 parts of tetrahydrofuran. Upon completion, stirring is continued for 1 hour at reflux temperature. The reaction mixture is cooled and poured onto a solution of 75 parts of ammonium chloride in water. The product is extracted with 2,2'-oxybispropane. The extract is washed with water, dried, filtered and evaporated, yielding 35 parts of (3-methylphenyl) (1-methyl-4-piperidinyl)methanone as an oily residue.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04342870
Quelldatensatzuspto-grants-1982_08
ORD IDord-7766b44aae14420995ee55d945992721
Quellennotizuspto-grants-1982_08