HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1419622Erstellt: 26. Oktober 2026
Ethanol → Benzoic acid, 2,4-dichloro-5-fluoro-, ethyl ester
https://huagongshe.com/reaction/1419622
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethanol | HCID 702 | — |
| Edukt | 2,4-Dichloro-5-fluorobenzoyl chloride | HCID 2736821 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | Benzoic acid, 2,4-dichloro-5-fluoro-, ethyl ester | HCID 13630722 | 90,8% |
Reaktionsschritte
A 25-mL round-bottom flask was equipped with a magnetic stir bar, thermometer, nitrogen inlet, addition funnel, and a reflux condenser. The flask was charged with 2,4-dichloro-5-fluorobenzoyl chloride (5.38 g, 23.65 mmol) and ethyl ether (5.0 g). The resulting colorless solution was cooled to 17° C. using a cool water bath. Ethanol (3.20 g, 69.47 mmol; absolute grade) was added dropwise from the addition funnel over ten minutes. Once the addition was complete, the solution was warmed to room temperature and stirred overnight (17 hours). Additional ether (20 mL) was added to the reaction mixture, which was then transferred to a separatory funnel. The reaction mixture was washed twice with 2% sodium hydroxide solution (10 mL), then with water (10 mL). The upper organic layer was separated and dried over sodium sulfate. The solvent was removed by evaporation under reduced pressure. The residue was dried in a vacuum oven to give 5.09 g of ethyl 2,4-dichloro-5-fluorobenzoate as a pale yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05886210 |
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| Quelldatensatz | uspto-grants-1999_03 |
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| ORD ID | ord-58ddac9ecb2b4652b575a9e3beaa407b |
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| Quellennotiz | uspto-grants-1999_03 |
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