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HRID 617001作成日:2026年10月27日

Sodium Carbonate → 1-(4,4-Diphenylcyclohexyl)-4-(4-chloro-3-trifluoromethylphenyl)-4-piperidinol hydrochloride monohydrate

https://huagongshe.com/reaction/617001

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物4-(4-Chloro-3-(trifluoromethyl)phenyl)piperidin-4-olHCID 89107—
反応物4,4-Diphenylcyclohexyl tosylateHCID 20366912—
溶媒TolueneHCID 1140—
生成物1-(4,4-Diphenylcyclohexyl)-4-(4-chloro-3-trifluoromethylphenyl)-4-piperidinol hydrochloride monohydrateHCID 20366934—

反応手順

A mixture of 4.1 g of 4,4-diphenylcyclohexyl tosylate, 2.8 g of 4-(4-chloro-3-trifluoromethylphenyl)-4-piperidinol, 1.1 g of sodium carbonate and 400 ml of toluene is stirred under reflux for 48 hours. The reaction mixture is concentrated completely under reduced pressure, water is added to the residue, and the aqueous mixture is extracted with chloroform. The extract is washed with water and dried over sodium sulfate, and the solvent is removed. The esidual viscous oil is purified by column chromatography on silica gel using chloroform and then chloroform - methanol (9:1) as an eluent. The purified base is converted in a conventional manner into the hydrochloride. Thus is obtained 1-(4,4-diphenylcyclohexyl)-4-(4-chloro-3-trifluoromethylphenyl)-4-piperidinol hydrochloride monohydrate as white crystals, melting at 270°-273° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04076821
出典データセットuspto-grants-1978_02
ORD IDord-6b2e2ad3436c4cc69ba735545e7b983b
出典メモuspto-grants-1978_02