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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579328Generated: November 3, 2026

Potassium Iodide → HCID 21568339, compound

https://huagongshe.com/reaction/1579328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium BicarbonateHCID 516893—
Reactant4'-tert-Butyl-4-chlorobutyrophenoneHCID 2723694—
ReactantHCID 12795120HCID 12795120—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 21568339HCID 21568339—

Reaction Steps

A mixture of 11 g (0.035 mole) of α-phenyl-α-(p-chlorophenyl)-4-piperidinemethanol, 12.5 g (0.05 mole) of 4'-tert-butyl-4-chlorobutyrophenone, 10 g of potassium bicarbonate, 0.1 g of potassium iodide, 100 ml of toluene and 10 ml of water is refluxed with stirring for about 93 hours. Upon cooling to room temperature the mixture is filtered and the toluene layer is separated. The aqueous layer is extracted with toluene. The combined organic fractions are washed with water and saturated sodium chloride solution, dried over magnesium sulfate, and filtered. To the filtrate is added an equal volume of ether followed by treatment with ethereal HCl. The resulting precipitate is collected and recrystallized from methanol-butanone to give 4'-tert-butyl-4-[4-[α-hydroxy-α-(p-chlorophenyl)benzyl]-piperidino]butyrophenone hydrochloride, M.P. 238.5°-240°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931197
Source datasetuspto-grants-1976_01
ORD IDord-7308669c48824978b118ea29e628ebca
Source noteuspto-grants-1976_01