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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 624863Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/624863

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktCesium carbonateHCID 10796—
EduktPotassium cyclopropyltrifluoroborateHCID 23697338—
Edukt5-Bromo-6-(1,1,1-trifluoropropan-2-yloxy)picolinic acidHCID 71087582—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorButyl-1-adamantylphosphineHCID 68995490—
LösungsmittelTolueneHCID 1140—
Produkt5-Cyclopropyl-6-(1,1,1-trifluoropropan-2-yloxy)picolinic acidHCID 7108743579%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

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]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09303012B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-f8f51eff5cd34051872e2767fc006127
Quellennotizuspto-grants-2016_04