HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 241981Erstellt: 24. Oktober 2026
Hydrochloric Acid → Ethyl 3-(2,6-difluorophenyl)-3-oxopropanoate
https://huagongshe.com/de/reaction/241981
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 2,6-Difluorobenzoic acid | HCID 9796 | — |
| Edukt | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Edukt | Potassium ethyl malonate | HCID 3446434 | — |
| Edukt | Magnesium Chloride | HCID 5360315 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Ethyl 3-(2,6-difluorophenyl)-3-oxopropanoate | HCID 13550002 | — |
Reaktionsschritte
A mixture of 2,6-difluorobenzoic acid (15 g, 0.095 mol) and carbonyldiimidazole (18 g, 0.14 mol, 1.5 equiv) in anhydrous tetrahydrofuran (150 mL) was stirred at ambient temperature for 6 hours. In a separate flask, a suspension of anhydrous magnesium(II) chloride (9.0 g, 0.095 mol, 1.0 equiv) and potassium ethyl malonate (22 g, 0.13 mol, 1.4 equiv) in tetrahydrofuran (225 mL) was stirred at 50-60° C. for 6 hours, cooled to ambient temperature, which was then added via syringe to the solution of activated acid, and the mixture was stirred for an additional 18 hours at ambient temperature. The mixture was refluxed for 3 hours, cooled to ambient temperature, poured into water and acidified with hydrochloric acid (12 N aqueous) to pH<2. The aqueous layer was extracted with ethyl acetate and the organic extract was washed with water, dried with sodium sulfate, filtered and concentrated in vacuo, providing the titled compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08653079B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-aa0c7c90c9db4181bb4de98653e3f5ed |
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| Quellennotiz | uspto-grants-2014_02 |
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