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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-((5-Chloro-3-fluoro-2-pyridinyl)oxy)phenol | HCID 15592838 | — |
| Reactant | 2-Bromopropionic acid N-cyano-N-methylamide | HCID 53744792 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-[4-(5-chloro-3-fluoropyridin-2-yloxy)phenoxy]propionic acid N-cyano-N-methylamide | HCID 54469043 | 87.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04759796 |
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| Source dataset | uspto-grants-1988_07 |
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| ORD ID | ord-fc15e6acc0a44fef85849122ee436e2f |
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| Source note | uspto-grants-1988_07 |
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