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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 632452Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/632452

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
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—
LösungsmittelWaterHCID 962—
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 icewater/1N HCl (150 mL) and extracted with EtOAc (2×300 mL). The combined organic layers were washed with icewater/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
PatentnummerUS09321727B2
Quelldatensatzuspto-grants-2016_04
ORD IDord-ae0dddf6dcb44928a58fb06af65a7bda
Quellennotizuspto-grants-2016_04