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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816660Generated: October 26, 2026

Iodoethane → 2-Ethoxy-4-(trifluoromethyl)benzaldehyde

https://huagongshe.com/reaction/1816660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Hydroxy-4-(trifluoromethyl)benzaldehydeHCID 22493901—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-Ethoxy-4-(trifluoromethyl)benzaldehydeHCID 2249433865.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

0.80 g of 2-hydroxy-4-(trifluoromethyl)benzaldehyde was dissolved in 8 ml dimethylformamide, and 0.78 g of ethyl iodide and 0.69 g of potassium carbonate were added, and the mixture was stirred at 70° C. for 2 hours. The reaction solution was diluted with water and then extracted with ethyl acetate. The organic layer was successively washed with 1N hydrochloric acid and brine, dried over anhydrous magnesium sulfate and the solvent was evaporated. The residue was subjected to silica gel column chromatography, and from fractions eluted with hexane-ethyl acetate (5:1), 0.60 g of 2-ethoxy-4-(trifluoromethyl)benzaldehyde was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884821B1
Source datasetuspto-grants-2005_04
ORD IDord-3ab593fd741744e0a05f036f523515f4
Source noteuspto-grants-2005_04