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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 269591생성일: 2026년 10월 24일

Hydrochloric Acid → 6''Fluoro-2-benzyloxy-[1,1':2',1'']terphenyl-3''-carboxylic acid

https://huagongshe.com/ko/reaction/269591

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium CarbonateHCID 11430—
반응물3-Bromo-4-fluorobenzoic acidHCID 70509—
반응물2'-Benzyloxy-biphenyl-2-boronic acidHCID 58730990—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물6''Fluoro-2-benzyloxy-[1,1':2',1'']terphenyl-3''-carboxylic acidHCID 44581655—

반응 조건

온도90 °C

반응 단계

{2′-[(phenylmethyl)oxy]-2-biphenylyl}boronic acid (60 mg, 0.19 mmol) and 3-bromo-4-fluorobenzoic acid (69 mg, 0.31 mmol) were dissolved in 1:1 toluene:ethanol (6 ml) under nitrogen. Potassium carbonate (290 mg, 2.1 mmol) and tetrakis(triphenylphosphine)palladium(0) (23 mg, 0.019 mmol) were added and the mixture heated at 90° C. for 1 h. After cooling, the reaction mixture was poured into water, acidified with 1M HCl solution and extracted with ethyl acetate (15×2 ml), the combined organic layer were dried and evaporated. The residue was then purified on an SPE column using 40% of ethyl acetate in iso-hexane to give the title compound as white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07446222B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-87b199b644b94a979230c2456be54945
출처 메모uspto-grants-2008_11