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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762397Generated: November 1, 2026

Potassium Carbonate → Methyl (2R)‐2‐{4‐[(5‐chloro‐3‐fluoropyridin‐2‐ yl)oxy]phenoxy}propanoate

https://huagongshe.com/reaction/1762397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-((5-Chloro-3-fluoro-2-pyridinyl)oxy)phenolHCID 15592838—
Reactant(S)(-)-lactic acid-methylester tosylateHCID 86743051—
SolventDimethyl SulfoxideHCID 679—
ProductMethyl (2R)‐2‐{4‐[(5‐chloro‐3‐fluoropyridin‐2‐ yl)oxy]phenoxy}propanoateHCID 15592837—

Reaction Steps

A solution of 24 g (0.1 mol) of 4-(5-chloro-3-fluoropyridin-2-yloxy)-phenol in 80 ml of dimethylsulfoxide is added dropwise to a stirred solution of 13.8 g (0.1 mol) of potassium carbonate in 50 ml of dimethylsulfoxide. When everything is added, the mixture is stirred for 2 hours at room temperature and then 25.8 g (0.1 mol) of (S)(-)-lactic acid-methylester tosylate is added dropwise over 30 minutes. The mixture is heated to 60° and stirred at that temperature for 20 hours, then poured onto ice/water and the organic material is extracted three times with ether. The ether-layer is washed with water and saturated salt solution, dried over magnesium sulfate, filtered and evaporated. The residue is passed for purification through a silicagel column with a hexane/ethyl acetate 3:1 solvent. After distillation of the solvent, 26 g of a clear oil of the above ester is obtained ([α]D20 =+38.8±0.5° 2% in acetone).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04832736
Source datasetuspto-grants-1989_05
ORD IDord-ae2044c80a1f4f0393ba40349cda59bd
Source noteuspto-grants-1989_05