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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2083671Erstellt: 24. Oktober 2026

Potassium Iodide → 2,2-Diphenyl-4-piperidin-1-ylbutanenitrile

https://huagongshe.com/reaction/2083671

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
EduktPiperidineHCID 8082—
Edukt4-Bromo-2,2-diphenylbutyronitrileHCID 96575—
EduktPotassium BicarbonateHCID 516893—
LösungsmittelWaterHCID 962—
Produkt2,2-Diphenyl-4-piperidin-1-ylbutanenitrileHCID 22457766,6%

Reaktionsschritte

1.96 Parts piperidine, 1.91 parts potassium iodide and 25 parts deionized water are combined and gently heated under a nitrogen atmosphere. To this slurry is then added 2.75 parts of potassium bicarbonate, followed by 7.51 parts of 2,2-diphenyl-4-bromobutyronitrile. The mixture is heated to reflux and maintained thereat for 4.5 hours. After cooling to room temperature, the reaction mixture is extracted three times with 14 part portions of ethyl ether. The ether extracts are combined, and extracted six times with 25 parts by volume portions of dilute acetic acid solution. The acid extracts are combined, basified to about pH 10 - 12 with 50% sodium hydroxide solution, and again extracted with ethyl ether. The ether extracts are combined, washed with water and saturated sodium chloride solution, and dried over anhydrous potassium carbonate. Removal of the solvent affords 2,2-diphenyl-4-piperidinobutyronitrile, identical to the product of Example 22, in a 66.6% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04086234
Quelldatensatzuspto-grants-1978_04
ORD IDord-ac663a5a1f92405a993d0944f95d3bf9
Quellennotizuspto-grants-1978_04