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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44986생성일: 2026년 10월 23일

Morpholine → 4-(5-Bromopyridin-3-yl)morpholine

https://huagongshe.com/ko/reaction/44986

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물1,4-DioxaneHCID 31275—
반응물3,5-DibromopyridineHCID 69369—
반응물Sodium t-butoxideHCID 23676156—
촉매HCID 178418397HCID 178418397—
생성물4-(5-Bromopyridin-3-yl)morpholineHCID 4673961441.1%

반응 조건

온도80 °C

반응 단계

To a solution of [3,5-dibromopyridine (1000 mg, 0.004 mol) in 1,4-dioxane (8 mL, 0.1 mol), morpholine (400 mg, 0.004 mol) and sodium tert-butoxide (400 mg, 0.004 mol) were added. The reaction was bubbled with nitrogen. Tetrakis(triphenylphosphine)palladium(0) (200 mg, 0.0002 mol) was added and nitrogen was bubbled through for couple of minutes. The mixture was heated at 80° C. overnight. The reaction was allowed to cool to rt and was then partitioned between water and ethyl acetate. The organic layer was washed with saturated sodium chloride, dried over magnesium sulfate, filtered and concentrated to give a crude residue. The crude product was purified by FCC on silica gel eluting with 1:1, EtOAC:Hexane gave to give 4-(5-bromopyridin-3-yl)morpholine as a viscous oil (400 mg, 40%). 1H NMR (400 MHz, CDCl3): 8.2 (s, 1H), 8.1 (s, 1H), 7.2 (s, 1H), 3.8 (m, 4H), 3.2 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541425B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-f68c61ed84274e17b1717f97a24de537
출처 메모uspto-grants-2013_09