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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30755생성일: 2026년 10월 24일

Cesium fluoride → 4'-(2-Hydroxyethoxy)-3',5'-dimethylbiphenyl-4-carboxylic acid

https://huagongshe.com/ko/reaction/30755

반응식

참여 물질

역할이름HCID투입량
반응물Cesium fluorideHCID 25953—
반응물1,4-DioxaneHCID 31275—
반응물4-Carboxyphenylboronic AcidHCID 312183—
반응물2-(4-Bromo-2,6-dimethylphenoxy)ethanolHCID 53707443—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물4'-(2-Hydroxyethoxy)-3',5'-dimethylbiphenyl-4-carboxylic acidHCID 2309073138.2%

반응 조건

온도90 °C

반응 단계

A mixture of 2-(4-bromo-2,6-dimethylphenoxy)ethanol (0.65 g), 4-carboxyphenylboronic acid (0.87 g), tetrakis(triphenylphosphine)palladium(0) (0.15 g), cesium fluoride (2.40 g), 1,4-dioxane (7.5 mL), ethanol (2.5 mL) and water (1.5 mL) was stirred at 90° C. overnight under an atmosphere of argon. Water and ethyl acetate were added to the reaction mixture. The organic layer was separated, washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent:ethyl acetate/n-hexane=1/1-2/1) to afford the title compound (0.29 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423185B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-29c629dfd82e403abf56ff372f921911
출처 메모uspto-grants-2008_09