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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17736생성일: 2026년 10월 23일

Ethyl Acetate → 4-(4-Chloro-3-ethylphenoxy)-1-nitrobenzene

https://huagongshe.com/ko/reaction/17736

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물p-FluoronitrobenzeneHCID 9590—
반응물Potassium CarbonateHCID 11430—
반응물4-Chloro-3-ethylphenolHCID 84223—
용매DimethylformamideHCID 6228—
생성물4-(4-Chloro-3-ethylphenoxy)-1-nitrobenzeneHCID 66977523—

반응 조건

온도80 °C

반응 단계

To a stirred solution of 1-fluoro-4-nitrobenzene (10 mmol) in DMF (20 mL) at rt, solid potassium carbonate (30 mmol) was added followed by addition of 4-chloro-3-ethylphenol (10 mmol) to the reaction mixture and heating to 80° C. until the reaction was complete as indicated by TLC or HPLC. After cooling to rt, the reaction mixture was poured into EtOAc (100 mL), washed with H2O (2×50 mL) and brine (50 mL), and dried over sodium sulfate. The solvent was removed in vacuuo to afford the desired 4-(4-chloro-3-ethylphenoxy)-1-nitrobenzene. The crude product was used for further transformation.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737285B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c9b591b7bdb2490a88e07295fec5b175
출처 메모uspto-grants-2010_06