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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17670생성일: 2026년 10월 23일

1-Fluoro-4-(4-nitrophenoxy)-2-(trifluoromethyl)benzene → 4-[4-Fluoro-3-(trifluoromethyl)phenoxy]aniline

https://huagongshe.com/ko/reaction/17670

반응식

참여 물질

역할이름HCID투입량
반응물1-Fluoro-4-(4-nitrophenoxy)-2-(trifluoromethyl)benzeneHCID 66977640—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물4-[4-Fluoro-3-(trifluoromethyl)phenoxy]anilineHCID 6697734495%

반응 단계

The nitro intermediate (2 mmol) obtained above was dissolved in MeOH (10 mL) and hydrogenated in the presence of 10% Pd/C (50 mg) until completion as indicated by TLC or LC-MS, according to General Procedure H. The reaction mixture was then filtered to remove the catalyst. The solvent was removed in vacuuo to afford 4-(4′-fluoro-3′-trifluoromethyl-phenoxy)aniline, which was used directly for further transformation without purification (overall yield: 95%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737285B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-836381fb90c949e58b19cd2c031e2a6b
출처 메모uspto-grants-2010_06