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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1270717생성일: 2026년 10월 26일

Potassium Carbonate → 2,3,5,6-Tetrafluoro-4-(3'-methoxyphenyl)aniline

https://huagongshe.com/reaction/1270717

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Tri-o-tolylphosphineHCID 80271—
반응물4-Bromo-2,3,5,6-tetrafluoroanilineHCID 618671—
반응물(3-Methoxyphenyl)boronic acidHCID 2734370—
촉매palladium(II) acetateHCID 167845—
용매1,2-DimethoxyethaneHCID 8071—
생성물2,3,5,6-Tetrafluoro-4-(3'-methoxyphenyl)anilineHCID 18451489—

반응 조건

온도90 °C

반응 단계

Alternative procedure: 2,3,5,6-Tetrafluoro-4-bromoaniline (12.0 g, 49.2 mmol) is dissolved in DME (250 mL) and treated with 3-methoxyphenylboronic acid (7.5 g, 49.2 mmol), a catalytic amount of palladium(II) acetate (0.23 g, 1.0 mmol) and tri-o-tolylphosphine (1.22 g, 4.0 mmol). Potassium carbonate (13.6 g in 50 mL water) is added and the reaction mixture stirred, purged with nitrogen, then heated to 90° C. for 24 hours. After cooling to room temperature most of the DME is removed by rotary evaporator under high vacuum. The resulting material is partitioned between EtOAc (200 mL) and water (250 mL). The organic layer is washed with brine, dried (Na2SO4) and concentrated by rotary evaporator. The crude reaction product is purified by flash chromatography (9:1 hexanes/EtOAc, then 6:4 hexanes/EtOAc) to give 2,3,5,6-tetrafluoro-4-(3′-methoxyphenyl)aniline (m.p. 94–96° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07202364B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-2811fa6bb2e04daaa00cb5e2387f1aa1
출처 메모uspto-grants-2007_04