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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Iodide | HCID 4875 | — |
| 反応物 | Azacyclonol | HCID 15723 | — |
| 反応物 | Potassium Bicarbonate | HCID 516893 | — |
| 反応物 | 4-Chloro-4'-cyclopentylbutyrophenone | HCID 13779253 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 4'-Cyclopentyl-4-[4-(alpha-hydroxy-alpha-phenylbenzyl)piperidino]butyrophenone hydrochloride | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US03931197 |
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| 出典データセット | uspto-grants-1976_01 |
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| ORD ID | ord-65064b1c45c344cc80de10238c77a32d |
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| 出典メモ | uspto-grants-1976_01 |
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