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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 567873생성일: 2026년 10월 26일

3,5-Dimethoxyphenol → 2-(3,5-Dimethoxyphenoxy)-6-fluorophenyl acetic acid

https://huagongshe.com/reaction/567873

반응식

참여 물질

역할이름HCID투입량
반응물3,5-DimethoxyphenolHCID 10383—
반응물Potassium CarbonateHCID 11430—
반응물2-Chloro-6-fluorophenylacetic acidHCID 123464—
촉매CopperHCID 23978—
촉매Copper iodideHCID 83717—
용매DimethylformamideHCID 6228—
생성물2-(3,5-Dimethoxyphenoxy)-6-fluorophenyl acetic acidHCID 5436934286.1%

반응 조건

온도120 °C

반응 단계

N,N-Dimethylformamide (20 ml) was added to 2-chloro-6-fluorophenyl acetic acid (3.77 g), 3,5-dimethoxyphenol (3.08 g), potassium carbonate (5.52 g), copper iodide (950 mg) and copper (250 mg), for stirring at 120° C. for 20 hours. The resulting solution was partitioned between ethyl acetate and dilute hydrochloric acid, and the organic phase was washed in water and in an aqueous saturated sodium chloride solution, and dried over anhydrous magnesium sulfate, to distill off the solvents under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: hexane:ethyl acetate=7:3), to recover 2-(3,5-dimethoxyphenoxy)-6-fluorophenyl acetic acid (5.27 g; yield of 86%). By 2H-NMR (90 MHz, CDCl3), the compound has the peaks shown below.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06180659B2
출처 데이터셋uspto-grants-2001_01
ORD IDord-efbdaef15b4a47079767403f833f42af
출처 메모uspto-grants-2001_01