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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105728Generated: October 31, 2026

Ethyl 2-chloropropionate → Ethyl 2-[4-[4-(trifluoromethyl)phenoxy]phenoxy]propanoate

https://huagongshe.com/reaction/1105728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-chloropropionateHCID 10807—
ReactantPotassium CarbonateHCID 11430—
Reactantp-(4-(Trifluoromethyl)phenoxy)phenolHCID 170230—
SolventMethyl Ethyl KetoneHCID 6569—
ProductEthyl 2-[4-[4-(trifluoromethyl)phenoxy]phenoxy]propanoateHCID 63192154%

Reaction Steps

A solution of 73.5 g of 4-(4-trifluoromethylphenoxy)phenol and 49.2 g of ethyl α-chloropropionate and 100 g of potassium carbonate were added to 100 ml of methyl ethyl ketone, and the mixture was heated. With stirring, the reaction was performed for 10 hours at the reflux temperature (80° to 85° C.). Inorganic salts were separated from the reaction product by filtration. The filtrate was evaporated and dried. The resulting ester was extracted with chloroform, and washed with water. The chloroform was distilled off to afford 55 g of the final product (yield: 54%). The final product had a boiling point of 176° to 185° C./3 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04309562
Source datasetuspto-grants-1982_01
ORD IDord-0180b70e8a9e4fb0a1e4ae74dd24f9d1
Source noteuspto-grants-1982_01