HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 430460Erstellt: 24. Oktober 2026
Ethyl Acetate → Ethyl 2-hydroxy-4-methyl-2-(trifluoromethyl)pent-4-enoate
https://huagongshe.com/de/reaction/430460
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 3-Bromo-2-methyl-1-propene | HCID 357785 | — |
| Edukt | Ethyl 3,3,3-trifluoro-2-oxopropanoate | HCID 2737239 | — |
| Katalysator | Manganese | HCID 23930 | — |
| Katalysator | Zincchloride | HCID 3007855 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Ethyl 2-hydroxy-4-methyl-2-(trifluoromethyl)pent-4-enoate | HCID 17935595 | — |
Reaktionsschritte
1.3 g of anhydrous zinc chloride and 13.2 g of granular manganese are heated to boiling in 100 ml of tetrahydrofuran and boiled with 0.2 ml of methallyl bromide for 30 minutes. Then, the solution of 25 g of methallylbromide and 17 g of trifluoropyruvic acid ethyl ester in 80 ml of tetrahydrofuran is added in drops at boiling heat over two hours and boiled for another hour. Then, it is added to saturated ammonium chloride solution and 300 ml of ethyl acetate while being cooled with ice, stirred for 30 minutes at 0° C., and the separated ethyl acetate phase is washed with saturated ammonium chloride solution and three times with water. The solvent is dried (Na2SO4) and concentrated by evaporation, and the residue is distilled in a vacuum. 17.6 g of 2-hydroxy-4-methylene-2-trifluoromethyl-valeric acid ethyl ester, boiling point 48° C., 1 hPa, is obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06323199B1 |
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| Quelldatensatz | uspto-grants-2001_11 |
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| ORD ID | ord-605ea9751b734934af7fb3bb1d09a996 |
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| Quellennotiz | uspto-grants-2001_11 |
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