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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 921016생성일: 2026년 10월 27일

2-Fluoro-4-nitroanisole → 1-Fluoro-4-(isocyanomethyl)-2-methoxy-5-nitrobenzene

https://huagongshe.com/reaction/921016

반응식

참여 물질

역할이름HCID투입량
반응물2-Fluoro-4-nitroanisoleHCID 223104—
반응물2-(4-Chlorophenoxy)acetonitrileHCID 306444—
반응물Potassium tert-butoxideHCID 23665647—
용매DimethylformamideHCID 6228—
생성물1-Fluoro-4-(isocyanomethyl)-2-methoxy-5-nitrobenzeneHCID 8671261924.4%

반응 단계

Potassium t-butoxide (15.74 g, 140 mmol) in DMF (50 mL) was added to a solution of 2-fluoro-1-methoxy-4-nitrobenzene (12 g, 70.1 mmol) and 2-(4-chlorophenoxyl)acetonitrile (11.75 g, 70.1 mmol) in DMF (100 mL) at −20° C. The reaction mixture was stirred for 1 h and then quenched with water. The aqueous layer was extracted with ethyl acetate. Organic layer was separated, washed with brine, dried over sodium sulphate, filtered and concentrated in vacuo. The crude product was purified by flash chromatography using 3% ethyl acetate in hexane to afford title compound (3.6 g, 23.21%) as a solid. 1H NMR (400 MHz, CDCl3): δ 8.05 (d, J=10.84 Hz, 1H), 7.27-7.23 (m, 1H), 4.28 (s, 2H), 4.05 (s, 3H); ESI-MS m/z=209 (M−H)−; LCMS Purity: 95%

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09273069B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-3bc4c05f356c41458847ae49013ab8ac
출처 메모uspto-grants-2016_03