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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615544Generated: October 25, 2026

Potassium Carbonate → 2-(4-Chlorobenzylthio)-ethyl 2-[4-(4-trifluoromethylphenoxy)-phenoxy]-propionate

https://huagongshe.com/reaction/615544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactantp-(4-(Trifluoromethyl)phenoxy)phenolHCID 170230—
Reactant2-{[(4-Chlorophenyl)methyl]sulfanyl}ethyl 2-bromopropanoateHCID 13309632—
SolventAcetonitrileHCID 6342—
Product2-(4-Chlorobenzylthio)-ethyl 2-[4-(4-trifluoromethylphenoxy)-phenoxy]-propionateHCID 1330960590.9%

Reaction Steps

A mixture consisting of 25.4 g of 4-(4-trifluoromethylphenoxy)phenol, 14.5 g of anhydrous potassium carbonate, 33.8 g of 2-(4-chlorobenzylthio)ethyl 2-bromopropionate and 150 ml of dry acetonitrile was refluxed for 3 hours with vigorous stirring. After cooling the reaction mixture to room temperature, the acetonitrile was removed under reduced pressure. Then, 150 ml of toluene were added to the residue and the resulting mixture was washed successively with 1% strength by weight aqueous sodium hydroxide solution and water, followed by dehydration. Upon distilling off the toluene under reduced pressure, there were obtained 46.4 g of 2-(4-chlorobenzylthio)-ethyl 2-[4-(4-trifluoromethylphenoxy)-phenoxy]-propionate in the form of a colorless oil. nD20 =1.5555.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04500346
Source datasetuspto-grants-1985_02
ORD IDord-47c941f55a7b4a46a403978b89ccb1da
Source noteuspto-grants-1985_02