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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 272486생성일: 2026년 10월 26일

Morpholine → 4-(6-Nitropyridin-3-yl)morpholine

https://huagongshe.com/reaction/272486

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물Potassium CarbonateHCID 11430—
반응물5-Bromo-2-nitropyridineHCID 817620—
촉매Tetrabutylammonium IodideHCID 67553—
용매Dimethyl SulfoxideHCID 679—
용매Ethyl AcetateHCID 8857—
생성물4-(6-Nitropyridin-3-yl)morpholineHCID 292797354.8%

반응 조건

온도80 °C

반응 단계

5-Bromo-2-nitropyridine (5.14 g, 25.3 mmol), tetra-n-butyl ammonium iodide (0.467 g, 1.27 mmol), morpholine (2.43 g, 27.9 mmol) and potassium carbonate (3.85 g, 27.9 mmol) were mixed in DMSO (50 mL). The reaction mixture was warmed to 80° C. for 15 hours. The reaction mixture was diluted with ethyl acetate and the solids removed by filtration. The organic filtrate was washed with water, then the solvent evaporated. The residue was then triturated with a dichloromethane/hexanes mixture to provide 4-(6-nitro-pyridin-3-yl)-morpholine as brown needles (2.90 g, 54.8%). 1H NMR δ(400 MHz, CDCl3) 8.16 (m, 1H), 7.97 (d, J=2.9 Hz, 1H), 7.15 (dd, J=3.2, 9.3 Hz, 1H), 3.45 (m, 4H), 1.72 (m, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456168B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-7d5b391c2a7041cd98f9b56ab1f1c162
출처 메모uspto-grants-2008_11