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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 624863생성일: 2026년 10월 26일

Water → 5-Cyclopropyl-6-(1,1,1-trifluoropropan-2-yloxy)picolinic acid

https://huagongshe.com/reaction/624863

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Cesium carbonateHCID 10796—
반응물Potassium cyclopropyltrifluoroborateHCID 23697338—
반응물5-Bromo-6-(1,1,1-trifluoropropan-2-yloxy)picolinic acidHCID 71087582—
촉매palladium(II) acetateHCID 167845—
촉매Butyl-1-adamantylphosphineHCID 68995490—
용매TolueneHCID 1140—
생성물5-Cyclopropyl-6-(1,1,1-trifluoropropan-2-yloxy)picolinic acidHCID 7108743579%

반응 조건

온도120 °C

반응 단계

5-Bromo-6-(1,1,1-trifluoropropan-2-yloxy)picolinic acid (2 g, 6.37 mmol), potassium cyclopropyltrifluoroborate (952 mg, 6.43 mmol), cesium carbonate (6.22 g, 19.1 mmol) and palladium(II)acetate (28.6 mg, 127 μmol) were suspended in toluene (55 mL) and water (6.11 mL) under an argon atmosphere. Butyl-1-adamantylphosphin (68.5 mg, 191 μmol) was added, the reaction mixture was heated to 120° C. for 1 d, poured onto ice-water/1N HCl (150 mL) and extracted with EtOAc (2×300 mL). The combined organic layers were washed with ice-water/brine (150 mL), dried over Na2SO4 and concentrated in vacuo to give the title compound (1.38 g, 79%) as a yellow solid. MS (EI): m/e=276.2 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09303012B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-f8f51eff5cd34051872e2767fc006127
출처 메모uspto-grants-2016_04