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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 242970생성일: 2026년 10월 26일

Aniline → (2-Nitropyridin-3-yl)phenylamine

https://huagongshe.com/reaction/242970

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참여 물질

역할이름HCID투입량
반응물AnilineHCID 6115—
반응물TriethylamineHCID 8471—
반응물3-Fluoro-2-nitropyridineHCID 2762802—
용매DimethylformamideHCID 6228—
생성물(2-Nitropyridin-3-yl)phenylamineHCID 20184004154.2%

반응 조건

온도100 °C

반응 단계

A mixture of 3-fluoro-2-nitropyridine (1.07 g, 6.75 mmol), aniline (1.8 mL, 20.2 mmol) and Et3N (2.8 mL, 20.2 mmol) in DMF (10 mL) was stirred at 100° C. for 16 h under a nitrogen atmosphere. After cooling to RT, the volatiles were removed under reduced pressure. The resulting residue was partitioned between DCM and water. The aqueous phase was further extracted with DCM (×3) and the combined organic fractions dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, gradient 0-4% MeOH in DCM) to afford the title compound as a red oil (2.24 g, quantitative). LCMS (Method C): RT 3.03 min [M+H]+ 216.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08653089B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-8f761dc54c3a4619aa346344671b6aeb
출처 메모uspto-grants-2014_02