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HRID 1579325作成日:2026年10月25日

Potassium Iodide → 4'-Cyclopentyl-4-[4-(alpha-hydroxy-alpha-phenylbenzyl)piperidino]butyrophenone hydrochloride

https://huagongshe.com/reaction/1579325

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物AzacyclonolHCID 15723—
反応物Potassium BicarbonateHCID 516893—
反応物4-Chloro-4'-cyclopentylbutyrophenoneHCID 13779253—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物4'-Cyclopentyl-4-[4-(alpha-hydroxy-alpha-phenylbenzyl)piperidino]butyrophenone hydrochlorideHCID 21568352—

反応手順

A mixture of 27.6 g (0.1 mole) of α,α-diphenyl-4-piperidinemethanol, 30 g (0.12 mole) of 4-chloro-4'-cyclopentylbutyrophenone, 20 g of potassium bicarbonate and 0.1 g of potassium iodide in 250 ml of toluene and 40 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 twice with 50 ml of 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 two volumes of ether, and the solution is treated with ethereal HCl. The resulting precipitate is collected and recrystallized from methanol-butanone to give 4'-cyclopentyl-4-[4-(α-hydroxy-α-phenylbenzyl)piperidino]butyrophenone hydrochloride, M.P. 232°-234°C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03931197
出典データセットuspto-grants-1976_01
ORD IDord-65064b1c45c344cc80de10238c77a32d
出典メモuspto-grants-1976_01