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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 411512생성일: 2026년 10월 25일

Fluorophenylacetic acid → 4-(4-Bromophenylsulphonyl)-1-(2-fluoro-2-phenylethyl)piperidine

https://huagongshe.com/reaction/411512

반응식

참여 물질

역할이름HCID투입량
반응물Fluorophenylacetic acidHCID 102649—
반응물4-(4-Bromobenzenesulfonyl)piperidineHCID 2761070—
생성물4-(4-Bromophenylsulphonyl)-1-(2-fluoro-2-phenylethyl)piperidineHCID 23499487—

반응 단계

4-(4-Bromophenylsulphonyl)piperidine (0.7 g, 2.3 mmol) was reacted with α-fluorophenylacetic acid (0.53 g, 3.45 mmol) in a similar manner as described for Example 13, Steps a and b, to give the required product as a colourless solid, 0.56 g (58%), m.p. 126-127° C. (EtOAc-pet. ether 60-80°). δH (400 MHz, CDCl3) 1.70-1.77 (2H, m), 2.00-2.03 (2H, m), 2.13-2.20 (2H, m), 2.57-2.69 (1H, m), 2.83-2.93 (2H, s), 3.04-3.18 (2H, m), 5.51-5.65 (1H, m), 7.28-7.39 (5H, m), 7.70-7.75 (4H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06559166B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-25390ca68c9e49bbaf1246d244e82f34
출처 메모uspto-grants-2003_05