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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359645Generated: October 30, 2026

Potassium Carbonate → Methyl 2-[4-(5-chloro-3-fluoropyridin-2-yloxy)phenoxy]propionate

https://huagongshe.com/reaction/359645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPropanoic acid, 2-(4-hydroxyphenoxy)-, methyl esterHCID 366926—
Reactant5-Chloro-2,3-difluoropyridineHCID 2783248—
Catalyst18-Crown-6HCID 28557—
SolventAcetonitrileHCID 6342—
ProductMethyl 2-[4-(5-chloro-3-fluoropyridin-2-yloxy)phenoxy]propionateHCID 1559283662.6%

Reaction Steps

To a stirred mixture of 21.6 g (0.11 mol) of 2-(4-hydroxyphenoxy)-propionic acid methyl ester, 15.2 g (0.11 mol) of potassium carbonate, 1.45 g (0.0055 mol) of 18-Crown-6 ether and 100 ml of acetonitrile is added dropwise a solution of 14.95 g (0.10 mol) of 5-chloro-2,3-difluoropyridine in 30 ml of acetonitrile and the mixture is heated at a temperature of 50° to 60° C. during 40 hours. The mixture is then poured into ice/water. The organic material is extracted with ethyl acetate, washed with a saturated salt solution, dried over magnesium sulfate, filtered and evaporated. The oily residue is purified by chromatography over a silica gel column with a hexane/ethyl acetate 3:1 solvent. After evaporation of the solvent one obtain 20.4 g of the above ester (63% of the theory) is obtained in crystalline form. The melting point is 63°-64° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05002604
Source datasetuspto-grants-1991_03
ORD IDord-797f56278f6a4c2b893d8a429875c6f1
Source noteuspto-grants-1991_03