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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1836338생성일: 2026년 10월 26일

Sodium Iodide → 4-(4-Bromophenylsulphonyl)-1-[2-(2,4-difluorophenyl)ethyl]piperidine

https://huagongshe.com/reaction/1836338

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Potassium CarbonateHCID 11430—
반응물4-(4-Bromobenzenesulfonyl)piperidineHCID 2761070—
반응물2,4-Difluorophenethyl bromideHCID 11298989—
용매AcetonitrileHCID 6342—
생성물4-(4-Bromophenylsulphonyl)-1-[2-(2,4-difluorophenyl)ethyl]piperidineHCID 1104851258.5%

반응 단계

A mixture of 4-(4-bromophenylsulphonyl)piperidine (7.6 g, 0.025 mol), 2,4-difluorophenethyl bromide (8.3 g, 0.38 mol), potassium carbonate (7.5 g, 0.054 mol) and sodium iodide (5.6 g, 0.037 mol) in CH3CN (70 ml) was heated at reflux under nitrogen for 18 h. The reaction mixture was then concentrated and partitioned between water and EtOAc. The organic phase was washed with brine, dried (Na2SO4) and concentrated. Trituration with hexane gave 6.5 g of product as a colourless solid. δH (360 MHz, CDCl3) 1.55-1.75 (2H, m), 1.95-2.05 (4H, m), 2.45-2.55 (2H, m), 2.70-2.75 (2H, m), 2.85-2.95 (1H, m), 3.05-3.10 (2H, m), 6.70-6.85 (2H, m), 7.10-7.15 (1H, m), 7.72 (4H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06777430B2
출처 데이터셋uspto-grants-2004_08
ORD IDord-f24e819cbe4249689051c30370095566
출처 메모uspto-grants-2004_08