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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632452Generated: October 25, 2026

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

https://huagongshe.com/reaction/632452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCesium carbonateHCID 10796—
ReactantPotassium cyclopropyltrifluoroborateHCID 23697338—
Reactant5-Bromo-6-(1,1,1-trifluoropropan-2-yloxy)picolinic acidHCID 71087582—
Catalystpalladium(II) acetateHCID 167845—
CatalystButyl-1-adamantylphosphineHCID 68995490—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product5-Cyclopropyl-6-(1,1,1-trifluoropropan-2-yloxy)picolinic acidHCID 7108743579%

Reaction Conditions

Temperature120 °C

Reaction Steps

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]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321727B2
Source datasetuspto-grants-2016_04
ORD IDord-ae0dddf6dcb44928a58fb06af65a7bda
Source noteuspto-grants-2016_04