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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 467064생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/467064

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Potassium CarbonateHCID 11430—
반응물3-BromopropionitrileHCID 17020—
반응물Paroxetine HydrochlorideHCID 62878—
용매AcetoneHCID 180—
용매Diethyl EtherHCID 3283—
생성물(-)-trans-1(2-Cyanoethyl)-4-(4-fluorophenyl)-3-(3,4-methylenedioxyphenoxymethyl)-piperidine hydrochlorideHCID 67638429—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05158961
출처 데이터셋uspto-grants-1992_10
ORD IDord-eb66a0f4ae404633a525c7dfed23e0e5
출처 메모uspto-grants-1992_10