Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155788Generated: October 25, 2026

Phenol → 2-{4-[2-Chloro-4-(trifluoromethyl)phenoxy]phenoxy}propanoic acid

https://huagongshe.com/reaction/1155788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantSodium CarbonateHCID 10340—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloropropionic acidHCID 11734—
Reactant4-[2-Chloro-4-(trifluoromethyl)phenoxy]phenolHCID 12940613—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product2-{4-[2-Chloro-4-(trifluoromethyl)phenoxy]phenoxy}propanoic acidHCID 12906017—

Reaction Steps

28.9 g of 4-(2-chloro-4-trifluoromethylphenoxy)phenol was added to 50 ml of dioxane, and with stirring at 30° to 40° C., 13.8 g of potassium carbonate was added. The mixture was heated to 40° to 60° C., and 10.8 g of α-chloropropionic acid was added. The reaction was performed for 4 hours. The disappearance of the starting phenol was confirmed by gas chromatography, and the reaction product was poured into a suitable amount of water. Sodium carbonate was added to transfer the final product into the aqueous phase. The oily phase was separated and removed, and then hydrochloric acid was added to afford 20 g of a solid precipitate. The final product obtained had a melting point of 90° to 92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04332961
Source datasetuspto-grants-1982_06
ORD IDord-cef4036760bb48da882fde5cdfc02e10
Source noteuspto-grants-1982_06