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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 603336생성일: 2026년 10월 26일

Hydrochloric Acid → N-(4-Ethylphenyl)-2,3,5,6-tetrafluoroaniline

https://huagongshe.com/reaction/603336

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2,3,5,6-TetrafluoroanilineHCID 12786—
반응물1-Bromo-4-ethylbenzeneHCID 15313—
반응물Tris(1,1-dimethylethyl)phosphineHCID 83681—
반응물Sodium t-butoxideHCID 23676156—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물N-(4-Ethylphenyl)-2,3,5,6-tetrafluoroanilineHCID 21938675—

반응 조건

온도85 °C

반응 단계

A mixture of 2,3,5,6-tetrafluoroaniline (4.5 g, 27.3 mmol), 4-ethylbromobenzene (5.0 g, 27 mmol), toluene (50 ml), sodium tert-butoxide (4.67 g, 48 mmol), tri-tert-butylphosphin (217 mg, 1.07 mmol) and bis-dibenzylideneacetone-palladium(0) (260 mg, 0.45 mmol) is heated under nitrogen to 85° C. for 15.5 h. The mixture is cooled to room temperature and water (30 ml), concentrated hydrochloric acid (20 ml) and hyflo are added. After stirring for 45 minutes, the mixture is filtered and the organic phase is washed with water three times. The solvent is evaporated in vacuo and the residue is chromatographed on silica using hexane/toluene (9:1 to 3:1) affording N-(2′,3′,5′,6′-tetrafluorophenyl)-4-ethylanilin as a liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07906677B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-db7c28842a0549feb90e747c0c7962f1
출처 메모uspto-grants-2011_03