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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13501생성일: 2026년 10월 24일

p-Fluoronitrobenzene → Methyl 5-(4-nitrophenoxy)pyridine-3-carboxylate

https://huagongshe.com/ko/reaction/13501

반응식

참여 물질

역할이름HCID투입량
반응물p-FluoronitrobenzeneHCID 9590—
반응물Potassium CarbonateHCID 11430—
반응물Methyl 5-hydroxypyridine-3-carboxylateHCID 354317—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
용매DimethylformamideHCID 6228—
생성물Methyl 5-(4-nitrophenoxy)pyridine-3-carboxylateHCID 22040734—

반응 조건

온도80 °C

반응 단계

The mixture containing methyl-5-hydroxypyridine-3-carboxylate (1 eq), Potassium bis(trimethylsilyl)amide (1.2 eq) was stirred in N,N-dimethylformamide for 2 hours at room temperature. To this mixture was added 1-fluoro-4-nitrobenzene (1.1 eq) and Potassium carbonate (1.2 eq) and stirred at 80° C. for 16 h. The reaction mixture was then concentrated and partitioned between ethyl acetate and water. The organic layer was separated and washed with brine, dried, filtered and concentrated in vacuum to give brown solid. Purification on silica gel methyl-5-(4-nitrophenoxy)pyridine-3-carboxylate. MS: MH+=274.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728010B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-827bc1173d3441568cf390f6559fafd8
출처 메모uspto-grants-2010_06