돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 703845생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/703845

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물1-BromopentaneHCID 8057—
반응물Potassium CarbonateHCID 11430—
반응물Paroxetine HydrochlorideHCID 62878—
용매EthanolHCID 702—
용매Diethyl EtherHCID 3283—
생성물(-)-trans-4-(-4-Fluorophenyl)-3-(3,4-methylenedioxyphenoxymethyl)-1-pentylpiperidine hydrochlorideHCID 66923321—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04985446
출처 데이터셋uspto-grants-1991_01
ORD IDord-0652fd7776f24f57a4347f8fc28f0b94
출처 메모uspto-grants-1991_01