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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384148Generated: October 25, 2026

Ethyl Acetate → 2-Chloro-1-(4-iodophenoxy)-4-(trifluoromethyl)benzene

https://huagongshe.com/reaction/384148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4-IodophenolHCID 10894—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzene, 2-chloro-1-fluoro-4-(trifluoromethyl)-HCID 157153—
SolventDimethyl SulfoxideHCID 679—
Product2-Chloro-1-(4-iodophenoxy)-4-(trifluoromethyl)benzeneHCID 68430723—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 4-iodophenol (200 mg) in dimethylsulfoxide (1 ml), 218 mg of 2-chloro-1-fluoro-4-(trifluoromethyl)benzene and 251 mg of potassium carbonate were added, and the reaction solution was stirred at 120° C. for 3 hours. The reaction solution was cooled, ethyl acetate was added, the insoluble matter was filtered off, and the filtrate was washed with water and a saturated saline solution and dried over an anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue obtained was purified by silica gel column chromatography (eluent: hexane/ethyl acetate (98:2-80/20)) to afford the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367708B2
Source datasetuspto-grants-2013_02
ORD IDord-236a00b7ed9d4ccda644ca54e62e3c55
Source noteuspto-grants-2013_02