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HRID 467064作成日:2026年10月26日

Ethanol → (-)-trans-1(2-Cyanoethyl)-4-(4-fluorophenyl)-3-(3,4-methylenedioxyphenoxymethyl)-piperidine hydrochloride

https://huagongshe.com/reaction/467064

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Potassium CarbonateHCID 11430—
反応物3-BromopropionitrileHCID 17020—
反応物Paroxetine HydrochlorideHCID 62878—
溶媒AcetoneHCID 180—
溶媒Diethyl EtherHCID 3283—
生成物(-)-trans-1(2-Cyanoethyl)-4-(4-fluorophenyl)-3-(3,4-methylenedioxyphenoxymethyl)-piperidine hydrochlorideHCID 67638429—

反応手順

1 g of (-)-trans-4-(4-fluorophenyl)-3-(3,4-methylene dioxyphenoxymethyl)-piperidine hydrochloride in 50 ml 99 9% ethanol was mixed with 3-bromopropionitrile (7 ml) and 2 g potassium carbonate. The mixture was refluxed for 70 h. After cooling 25 ml acetone and 25 ml diethylether were added, the precipitate filtered off, and the filtrate evaporated in vacuo. The residue was extracted with 1N NaOH/ether, the ether layer dried (MgSO4) and evaporated to dryness. The residue was dissolved in acetone and excess conc. HCl was added. Subsequent evaporation gave a hard glass, which was purified on a silica gel column using 99.5% ethanol as eluent. The title compound was isolated, and its structure confirmed by the IR and NMR data. M.p. 156° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05158961
出典データセットuspto-grants-1992_10
ORD IDord-eb66a0f4ae404633a525c7dfed23e0e5
出典メモuspto-grants-1992_10