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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083670Generated: October 26, 2026

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

https://huagongshe.com/reaction/2083670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPiperidineHCID 8082—
ReactantPotassium HydroxideHCID 14797—
Reactant4-Bromo-2,2-diphenylbutyronitrileHCID 96575—
SolventWaterHCID 962—
Product2,2-Diphenyl-4-piperidin-1-ylbutanenitrileHCID 22457786.1%

Reaction Steps

To 1.96 parts of piperidine is added 1.91 parts of potassium iodide and 25 parts deionized water under a nitrogen atmosphere. The mixture is gently warmed and 1.65 parts of potassium hydroxide and 7.51 parts of 2,2-diphenyl-4-bromobutyronitrile are added. The temperature is raised 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 four times with 25 parts by volume portions of a dilute acetic acid solution. The acid extracts are combined, neutralized to about pH 10 with 50% sodium hydroxide solution, and extracted again with ethyl ether. The ether extracts are combined, washed twice with 50 parts by volume portions of a saturated sodium chloride solution, and dried over anhydrous potassium carbonate. The solvent is removed under reduced pressure to afford, as an off-white solid, in 86.1% yield, 2,2-diphenyl-4-piperidinobutyronitrile. This compound melts at 74° - 77° C., and is represented by the following structural formula. ##STR16##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04086234
Source datasetuspto-grants-1978_04
ORD IDord-d64643250fdf4ac4984ab2f06ad440e5
Source noteuspto-grants-1978_04