HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 729362Erstellt: 25. Oktober 2026
Ethanol → Benzoic acid, 2,4,5-trifluoro-3-methoxy-, ethyl ester
https://huagongshe.com/reaction/729362
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 2,4,5-Trifluoro-3-methoxybenzoic acid | HCID 2733970 | — |
| Katalysator | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Benzoic acid, 2,4,5-trifluoro-3-methoxy-, ethyl ester | HCID 2774387 | 98,8% |
Reaktionsschritte
A solution of 2,4,5-trifluoro-3-methoxybenzoic acid (2.513 g, 12.19 mmol) in dichloromethane (50 mL) at 0° C. is treated with oxalyl chloride (5.4 mL, 61.9 mmol) followed by N,N-dimethylformamide (4 drops). The mixture is stirred at 0° C. for 5 minutes and then at room temperature for 2.5 hours. The mixture is concentrated to near dryness and then co-evaporated from benzene. The resulting acid chloride is diluted with dichloromethane (50 mL), cooled to 0° C., and then anhydrous ethanol (7.30 mL, 124 mmol) is added dropwise. The resulting solution is stirred at room temperature for 4.5 hours, poured into saturated NaHCO3 solution, and extracted with dichloromethane. The combined organic extracts are washed with brine, dried over Na2SO4, filtered, and concentrated under vacuum to afford the title compound as a light yellow liquid (2.82 g). 1H NMR (CDCl3): δ 7.47 (ddd, 1H), 4.39 (q, 2H), 4.05 (s, 3H), 1.40 (t, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07582627B2 |
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| Quelldatensatz | uspto-grants-2009_09 |
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| ORD ID | ord-276df7c94fad4fc6a9035df569eaef47 |
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| Quellennotiz | uspto-grants-2009_09 |
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