HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1051392Erstellt: 26. Oktober 2026
Potassium Hydroxide → 4,4,4-Trifluoro-3-formyl-butyric acid ethyl ester
https://huagongshe.com/reaction/1051392
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Edukt | Ethyl 4,4,4-trifluoro-3-(nitromethyl)butanoate | HCID 268363 | — |
| Edukt | Potassium Permanganate | HCID 516875 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4,4,4-Trifluoro-3-formyl-butyric acid ethyl ester | HCID 90103465 | — |
Reaktionsschritte
In a 100 mL round-bottomed flask, KOH (356 mg, 5.45 mmol) was combined with H2O (50 ml) to give a colorless solution and cooled to 0° C. 4,4,4-Trifluoro-3-nitromethyl-butyric acid ethyl ester (1.25 g, 5.45 mmol) in 10 ml THF was added and the resulting reaction mixture was stirred for 20 min. This was followed by addition of MgSO4 (657 mg, 5.45 mmol) in 5 ml of H2O then by KMnO4 (862 mg, 5.45 mmol) in 30 ml of H2O. The resulting reaction mixture was stirred for 30 min, filtered through celite and the celite cake washed with CH2Cl2. The combined filtrate and washes were washed with brine, dried over Na2SO4, filtered and concentrated to afford 4,4,4-trifluoro-3-formyl-butyric acid ethyl ester as a liquid which was used without purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09388172B2 |
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| Quelldatensatz | uspto-grants-2016_07 |
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| ORD ID | ord-955962637e704064a17b9764098c1f08 |
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| Quellennotiz | uspto-grants-2016_07 |
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