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HRID 267976생성일: 2026년 10월 26일

Potassium Iodide → 4'-Tert-butyl-6-[4-(alpha-hydroxy-alpha-phenylbenzyl)piperidino]caprophenone hydrochloride

https://huagongshe.com/reaction/267976

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물AzacyclonolHCID 15723—
반응물Potassium BicarbonateHCID 516893—
반응물4'-Tert-butyl-6-chlorocaprophenoneHCID 21552993—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물4'-Tert-butyl-6-[4-(alpha-hydroxy-alpha-phenylbenzyl)piperidino]caprophenone hydrochlorideHCID 21552957—

반응 단계

A mixture of 22.4 g (0.08 mole) of α,α-diphenyl-4-piperidinemethanol, 23.8 g (0.09 mole) of 4'-tert-butyl-6-chlorocaprophenone, 20 g (0.2 mole) of potassium bicarbonate, 0.1 g of potassium iodide in 300 ml of toluene and 45 ml of water is stirred on a steam bath for about 96 hours after which the organic layer is separated and combined with 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 ether and made acidic with ethereal HCl. The resulting precipitate is recrystallized from methanol-butanone to give 4'-tert-butyl-6-[4-(α-hydroxy-α-phenylbenzyl)piperidino]caprophenone hydrochloride.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03946022
출처 데이터셋uspto-grants-1976_03
ORD IDord-0999aa34735c40f8adce64a580f06ea6
출처 메모uspto-grants-1976_03