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HRID 703845作成日:2026年10月26日

Acetone → (-)-trans-4-(-4-Fluorophenyl)-3-(3,4-methylenedioxyphenoxymethyl)-1-pentylpiperidine hydrochloride

https://huagongshe.com/reaction/703845

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物1-BromopentaneHCID 8057—
反応物Potassium CarbonateHCID 11430—
反応物Paroxetine HydrochlorideHCID 62878—
溶媒EthanolHCID 702—
溶媒Diethyl EtherHCID 3283—
生成物(-)-trans-4-(-4-Fluorophenyl)-3-(3,4-methylenedioxyphenoxymethyl)-1-pentylpiperidine hydrochlorideHCID 66923321—

反応手順

10g of (-)-trans-4-(-4-fluorophenyl)-3-(3,4-methylenedioxy-phenoxymethyl)-piperidine hydrochloride in 250 ml 99.9% ethanol was mixed with 50 ml 1-bromopentane and 20 g potassium carbonate. The mixture was refluxed for 3 hours and was subsequently cooled to room temperature. 25 ml acetone and 25 ml diethylether was added to the solution. The precipitate was filtered off and the filtrate was evaporated in vacuo. 20 ml 4N NaOH was added to the residue, and the resulting mixture was extracted 3 times with diethyl ether. The combined ether phases were dried over potassium carbonate, filtered, the filtrate was acidified with conc. hydrochloric acid to pH 2, and the filtrate was evaporated in vacuo. The resulting oil was dissolved in acetone and crystals precipitated by addition of ether and after cooling at 4° C. over night. The title compound was filtered off and dried giving 10.1 g of the title compound. M.p. 153.6° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04985446
出典データセットuspto-grants-1991_01
ORD IDord-0652fd7776f24f57a4347f8fc28f0b94
出典メモuspto-grants-1991_01