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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 335213생성일: 2026년 10월 23일

3-Morpholinophenol → 4-(3-(2-Nitropyridin-3-yloxy)phenyl)morpholine

https://huagongshe.com/ko/reaction/335213

반응식

참여 물질

역할이름HCID투입량
반응물3-MorpholinophenolHCID 141343—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
반응물3-Fluoro-2-nitropyridineHCID 2762802—
용매TetrahydrofuranHCID 8028—
생성물4-(3-(2-Nitropyridin-3-yloxy)phenyl)morpholineHCID 6699516973.1%

반응 조건

온도0 °C

반응 단계

In a 125 mL round-bottom flask, 3-morpholinophenol (0.91 g, 5.07 mmol) was dissolved in THF (40 mL). Solution was cooled to 0° C. and NaHMDS (5.07 mL, 5.07 mmol) (1M in THF) was added slowly. The mixture was agitated for 15 minutes and solution of 3-fluoro-2-nitropyridine (0.60 g, 4.22 mmol) in THF (5 mL) was added slowly. After agitating for 2 hours the solvent was evaporated and the residue dissolved in 100 mL of CH2Cl2 and washed with diluted sodium bicarbonate solution twice, dried over magnesium sulfate, filtered and evaporated. Crude material was purified by chromatography on silica gel, eluted with 25% ethyl acetate/Hexane to give the title compound (0.93 g, 72%) was obtained as thick red oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883828B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-00fe353d2b4d45f4b86eb8337e7e6ede
출처 메모uspto-grants-2014_11