HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2263996Erstellt: 26. Oktober 2026
Ethanol → Ethyl 2-ethoxy-4-(trifluoromethyl)benzoate
https://huagongshe.com/reaction/2263996
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Iodoethane | HCID 6340 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 2-Hydroxy-4-(trifluoromethyl)benzoic acid | HCID 164578 | — |
| Produkt | Ethyl 2-ethoxy-4-(trifluoromethyl)benzoate | HCID 66857656 | 74% |
Reaktionsschritte
To a solution of 2-hydroxy-4-trifluoromethyl-benzoic acid (5 g, 24.258 mmol, Matrix Scientific) in ethanol (50 mL) were added potassium carbonate (8.38 g, 60.645 mmol) and ethyl iodide (7.68 mL, 97.032 mmol). The reaction mixture was heated at gentle reflux for 4 h then concentrated in vacuo. The residue was taken in petroleum ether and water, and the layers were separated. The product was extracted with petroleum ether (1×). The organic layers were washed with brine (1×), dried over anhydrous sodium sulfate, filtered and concentrated. Purification of the crude residue by flash chromatography (40 g of silica gel, eluting with 10% ethyl acetate in hexane) gave 2-ethoxy-4-trifluoromethyl-benzoic acid ethyl ester as colorless oil (4.68 g, 74%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07851626B2 |
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| Quelldatensatz | uspto-grants-2010_12 |
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| ORD ID | ord-ffcb9308274d4c01b5ea162c5ded78cb |
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| Quellennotiz | uspto-grants-2010_12 |
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