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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3687생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/3687

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 reaction solution was partitioned with ethyl acetate and dilute hydrochloric acid, and the organic phase was washed in water and in a 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 1H-NMR (90 MHz, CDCl3), the compound has the peaks shown below.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05734067
출처 데이터셋uspto-grants-1998_03
ORD IDord-83441b5019214471922280f5515c2e22
출처 메모uspto-grants-1998_03