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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12370생성일: 2026년 10월 25일

Water → 4-[2-(4-Fluorophenyl)ethylidene]-piperidine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/12370

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Benzyl 4-oxopiperidine-1-carboxylateHCID 643496—
반응물4-Fluorophenethyltriphenylphosphonium bromideHCID 22386745—
용매TetrahydrofuranHCID 8028—
생성물4-[2-(4-Fluorophenyl)ethylidene]-piperidine-1-carboxylic acid benzyl esterHCID 5742604217.2%

반응 단계

To a suspension of phosphonium bromide 78NLS66 (4.69 g, 10.1 mmol) in THF (100 mL) n-butyllithium (1.6 M in hexane, 6.3 mL, 10.1 mmol) was added at 0° C., giving a deep red solution. After stirring for 1 h at rt, a solution of benzyl 4-oxo-1-piperidinecarboxylate (2.24 g, 9.6 mmol) in THF (10 mL) was added dropwise over 30 min. The mixture was stirred at rt for 20 h, then water was added and the mixture extracted three times with diethylether. The combined organic layers were dried over Na2SO4, filtered and concentrated in vacuo. Purification of the residue by silica gel column chromatography, eluting with a stepwise gradient of 0-10% ethyl acetate in n-heptane, afforded the title compound (0.56 g, 17%) as a colourless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727999B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-82c7cda0ea19489b8bb5ea8f54195000
출처 메모uspto-grants-2010_06