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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845699Generated: October 27, 2026

Potassium Carbonate → 2-[4-(5-chloro-3-fluoropyridin-2-yloxy)phenoxy]propionic acid N-cyano-N-methylamide

https://huagongshe.com/reaction/845699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-((5-Chloro-3-fluoro-2-pyridinyl)oxy)phenolHCID 15592838—
Reactant2-Bromopropionic acid N-cyano-N-methylamideHCID 53744792—
CatalystPotassium IodideHCID 4875—
SolventAcetonitrileHCID 6342—
Product2-[4-(5-chloro-3-fluoropyridin-2-yloxy)phenoxy]propionic acid N-cyano-N-methylamideHCID 5446904387.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

48.0 g (0.20 mole) of 4-(5-chloro-3-fluoropyridin-2-yloxy)phenol and 38.2 g (0.20 mole) of 2-bromopropionic acid N-cyano-N-methylamide are dissolved in 400 ml of acetonitrile. 35.9 g (0.26 mole) of potassium carbonate and 0.33 g (0.002 mole) of potassium iodide are added to the solution and the reaction mixture is heated for 13 hours at 80° C. The precipitate is removed by filtration, the filtrate is concentrated by evaporation and the residue is taken up in 500 ml of methlyene chloride. The solution is purified by treatment with activated carbon and filtration through silica gel. The filtrate is concentrated by evaporation and the residue is crystallised from a mixture of hexane and ethyl acetate, affording 61 g of 2-[4-(5-chloro-3-fluoropyridin-2-yloxy)phenoxy]propionic acid N-cyano-N-methylamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04759796
Source datasetuspto-grants-1988_07
ORD IDord-fc15e6acc0a44fef85849122ee436e2f
Source noteuspto-grants-1988_07