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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658663Generated: November 1, 2026

Potassium Iodide → 1-(4-tert-Butylphenyl)-4-{4-[hydroxy(diphenyl)methyl]piperidin-1-yl}butan-1-one--hydrogen chloride (1/1)

https://huagongshe.com/reaction/1658663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantAzacyclonolHCID 15723—
ReactantPotassium BicarbonateHCID 516893—
Reactant4'-tert-Butyl-4-chlorobutyrophenoneHCID 2723694—
SolventTolueneHCID 1140—
Product1-(4-tert-Butylphenyl)-4-{4-[hydroxy(diphenyl)methyl]piperidin-1-yl}butan-1-one--hydrogen chloride (1/1)HCID 12795122—

Reaction Steps

A mixture of 107 g (0.4 mole) of α,α -diphenyl-4-piperidinemethanol, 105 g (0.44 mole) of 4' -tert-butyl-4-chlorobutyrophenone, 70 g (0.7 mole) of potassium bicarbonate, and a small amount of potassium iodide in 600 ml of toluene was refluxed and stirred for 21/2 days then filtered. The filtrate was treated with charcoal, filtered through celite then treated with ethereal HCl. The resulting solid was recrystallized from methanol and isopropyl alcohol to give the desired product, M.P. 234°-235° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03965257
Source datasetuspto-grants-1976_06
ORD IDord-44d40c3bbc8b4091b50ba9e03fb52569
Source noteuspto-grants-1976_06