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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 404360생성일: 2026년 10월 26일

Potassium Carbonate → Methyl 2-(5,5-dimethyl-1-cyclopenten-1-yl)-5'-(ethyloxy)-2'-fluoro-1,1'-biphenyl-4-carboxylate

https://huagongshe.com/reaction/404360

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물5-Ethoxy-2-fluorophenylboronic Acid (contains varying amounts of Anhydride)HCID 16217468—
반응물Methyl 3-(5,5-dimethylcyclopent-1-enyl)-4-(trifluoromethylsulfonyloxy)benzoateHCID 57467618—
촉매HCID 178418397HCID 178418397—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물Methyl 2-(5,5-dimethyl-1-cyclopenten-1-yl)-5'-(ethyloxy)-2'-fluoro-1,1'-biphenyl-4-carboxylateHCID 5770582690%

반응 조건

온도90 °C

반응 단계

To a stirred solution of methyl 3-(5,5-dimethylcyclopent-1-enyl)-4-(trifluoromethylsulfonyloxy)benzoate T3.5 (0.400 g, 1.1 mmol) in DMF (4.00 mL) at 23° C. was added 5-ethoxy-2-fluorophenylboronic acid (0.29 g, 1.6 mmol, commercially available from Sigma-Aldrich, St. Louis, Mo., USA), potassium carbonate (0.44 g, 3.2 mmol), and then tetrakis(triphenylphosphine)palladium (0.12 g, 0.11 mmol). The mixture was heated to 90° C. and stirred for 21 hours. The mixture was then cooled to room temperature, diluted with brine, and extracted three times with EtOAc. After drying over anhydrous magnesium sulfate and filtering, the organic solvent was removed under reduced pressure and the product was then purified on silica gel (0-10% EtOAc in hexanes) to yield T25.1 as a colorless oil (0.350 g, 90% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08748462B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-60c23cb0cbfc4cc4bbc8fb5cba67ffe7
출처 메모uspto-grants-2014_06