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HRID 624863作成日:2026年10月27日

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

https://huagongshe.com/reaction/624863

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Cesium carbonateHCID 10796—
反応物Potassium cyclopropyltrifluoroborateHCID 23697338—
反応物5-Bromo-6-(1,1,1-trifluoropropan-2-yloxy)picolinic acidHCID 71087582—
触媒palladium(II) acetateHCID 167845—
触媒Butyl-1-adamantylphosphineHCID 68995490—
溶媒TolueneHCID 1140—
生成物5-Cyclopropyl-6-(1,1,1-trifluoropropan-2-yloxy)picolinic acidHCID 7108743579%

反応条件

温度120 °C

反応手順

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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09303012B2
出典データセットuspto-grants-2016_04
ORD IDord-f8f51eff5cd34051872e2767fc006127
出典メモuspto-grants-2016_04