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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54547생성일: 2026년 10월 23일

Water → 2-(1-(4-Fluorobenzyl)piperidin-4-yl)ethan-1-ol

https://huagongshe.com/ko/reaction/54547

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물p-Toluenesulfonic acidHCID 6101—
반응물4-FluorobenzaldehydeHCID 68023—
반응물4-PiperidineethanolHCID 73953—
용매BenzeneHCID 241—
생성물2-(1-(4-Fluorobenzyl)piperidin-4-yl)ethan-1-olHCID 10561862—

반응 단계

A mixture of 4-(2-hydroxyethyl)piperidine (21.5 g), 4-fluorobenzaldehyde (17.5 ml) and p-toluene sulfonic acid (3 mg) in benzene (200 ml) was refluxed with separating water as the benzene azeotrope. After 2 hours, the mixture was evaporated in vacuo. The residue was dissolved in methanol (200 ml) and sodium borohydride (6.3 g) was added thereto at 5° C. After stirring at ambient temperature for 1 hour, the mixture was evaporated in vacuo. 4N Hydrochloric acid (200 ml) was added to the residue and washed with ethyl acetate. The aqueous layer was made basic to pH 10 with potassium carbonate and extracted with ethyl acetate. The extract was washed with water and brine, and dried over magnesium sulfate, and evaporated in vacuo to give 1-(4-fluorobenzyl)-4-(2-hydroxyethyl)piperidine (32.0 g) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05622976
출처 데이터셋uspto-grants-1997_04
ORD IDord-81c94a8cf3a54d16a3ac4f055b91e857
출처 메모uspto-grants-1997_04