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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2083672Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/2083672

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 22457775,3%

Reaktionsschritte

To a warmed mixture of 1.96 parts piperidine, 1.91 parts potassium iodide and 25 parts deionized water under a nitrogen atmosphere is added 3.46 parts potassium bicarbonate and 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 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 75.3% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04086234
Quelldatensatzuspto-grants-1978_04
ORD IDord-f0824a4fd71640d1b36e68157487fe77
Quellennotizuspto-grants-1978_04