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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267973Generated: October 26, 2026

Potassium Iodide → 4'-Fluoro-5-[4-(alpha-hydroxy-alpha-phenylbenzyl)piperidino]valerophenone hydrochloride

https://huagongshe.com/reaction/267973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantAzacyclonolHCID 15723—
ReactantPotassium BicarbonateHCID 516893—
Reactant5-Chloro-1-(4-fluorophenyl)-1-oxopentaneHCID 12649794—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4'-Fluoro-5-[4-(alpha-hydroxy-alpha-phenylbenzyl)piperidino]valerophenone hydrochlorideHCID 21552952—

Reaction Steps

A mixture of 19.3 g (0.07 mole) of α,α -diphenyl-4-piperidinemethanol, 17.1 g (0.08 mole) of 5-chloro-4'-fluorovalerophenone, 20.0 g (0.2 mole) of potassium bicarbonate, and 0.1 g of potassium iodide in 250 ml of toluene and 35 ml of water is stirred on a steam bath for 70 hours. The organic layer is separated and combined with two 50 ml toluene extracts of the aqueous layer. The combined organic material is washed with water and saturated sodium chloride solution, dried over magnesium sulfate and filtered. The filtrate is diluted with about 200 ml of ether then made acidic with ethereal HCl. The resulting precipitate is recrystallized from methanol-butanone to give 4'-fluoro-5-[4-(α-hydroxy-α-phenylbenzyl)piperidino]valerophenone hydrochloride, M.P. 177°-179°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03946022
Source datasetuspto-grants-1976_03
ORD IDord-e7775154740c442a8bdbdf18ccfcf47a
Source noteuspto-grants-1976_03