HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816660Generated: October 26, 2026
Iodoethane → 2-Ethoxy-4-(trifluoromethyl)benzaldehyde
https://huagongshe.com/reaction/1816660
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Hydroxy-4-(trifluoromethyl)benzaldehyde | HCID 22493901 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Ethoxy-4-(trifluoromethyl)benzaldehyde | HCID 22494338 | 65.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06884821B1 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-3ab593fd741744e0a05f036f523515f4 |
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| Source note | uspto-grants-2005_04 |
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