Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579326Generated: November 2, 2026

Potassium Iodide → 4'-Tert-butyl-4-[4-[alpha-hydroxy-alpha-(p-tolyl)benzyl]-piperidino]butyrophenone hydrochloride

https://huagongshe.com/reaction/1579326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium BicarbonateHCID 516893—
Reactant4'-tert-Butyl-4-chlorobutyrophenoneHCID 2723694—
Reactantalpha-Phenyl-alpha-(p-tolyl)-4-piperidinemethanolHCID 21568361—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4'-Tert-butyl-4-[4-[alpha-hydroxy-alpha-(p-tolyl)benzyl]-piperidino]butyrophenone hydrochlorideHCID 21568342—

Reaction Steps

A mixture of 29.0 g (0.1 mole) of α-phenyl-α-(p-tolyl)-4-piperidinemethanol, 32 g (0.12 mole) of 4'-tert-butyl-4-chlorobutyrophenone, 20 g of potassium bicarbonate, 0.1 g of potassium iodide, 300 ml of toluene and 50 ml of water is stirred on a steam bath for 88 hours. Upon cooling to room temperature the toluene layer is separated, and the aqueous layer is extracted with toluene. The combined toluene fractions are washed with water and saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to an oil. The oily residue is dissolved in dry ether and filtered. The filtrate is treated with ethereal HCl, and the resulting precipitate is collected and recrystallized from methanol-butanone to give 4'-tert-butyl-4-[4-[α-hydroxy-α-(p-tolyl)benzyl]-piperidino]butyrophenone hydrochloride, M.P. 194°-196.5°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931197
Source datasetuspto-grants-1976_01
ORD IDord-70a8fd652fee4eeda76ee9724cbc3fc0
Source noteuspto-grants-1976_01