HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8472Erstellt: 23. Oktober 2026
Water → Diethyl [2,3,4-trifluoro[(1S)-2-hydroxy-1-methylethyl]anilino]methylenemalonate
https://huagongshe.com/de/reaction/8472
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | (2S)-2-(2,3,4-Trifluoroanilino)propanol | HCID 11401466 | — |
| Katalysator | Tetrahexylammonium chloride | HCID 80021 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Diethyl [2,3,4-trifluoro[(1S)-2-hydroxy-1-methylethyl]anilino]methylenemalonate | HCID 11485652 | 90,2% |
Reaktionsschritte
At room temperature, potassium hydroxide (330 mg) and tetrahexylammonium chloride (190.1 mg) were dissolved in DMF (15 ml). After adding a solution (5 ml) of (2S)-2-(2,3,4-trifluoroanilino)propanol (1 g, 99.8% ee) and diethylethoxymethylenemalonate (2.09 g) in DMF, the resultant mixture was stirred for 1 hour. After adding water, the liquid reaction mixture was extracted with a solvent mixture of ethyl acetate and n-hexane (3:2). The organic layer was washed with water and dried over anhydrous magnesium sulfate. After evaporating the solvent, IPE was added to the obtained residue and the mixture was stirred at 0° C. for 1 hour. The crystals thus precipitated were collected by filtration and the moist product thus obtained was dried under reduced pressure. Thus, the title compound (1.65 g, 99.8% ee) was obtained as colorless crystals. The 1H-NMR and IR spectral data of this product was identical with those of the compound obtained in Example 63.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07087778B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-ed8211677cac405d8fa028af6a5bb94f |
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| Quellennotiz | uspto-grants-2006_08 |
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