HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8456Erstellt: 23. Oktober 2026
Hydrochloric Acid → (2S)-2-(2,3,4-Trifluoroanilino)propanol
https://huagongshe.com/de/reaction/8456
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | Methyl (2S)-2-(2,3,4-trifluoroanilino)propionate | HCID 10125210 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Produkt | (2S)-2-(2,3,4-Trifluoroanilino)propanol | HCID 11401466 | 84,1% |
Reaktionsschritte
Under ice-cooling, sodium borohydride (1.2 g) was dissolved in IPA (50 ml). After adding methanol (5 ml), a solution of the compound (5.0 g) obtained in Example 1 in IPA was dropped therein to. Then the liquid reaction mixture was heated to 50° C. and stirred for 1 hour. Next, hydrochloric acid (1 mol/l) was added and the mixture was stirred for a while. Then a saturated aqueous solution of sodium hydrogencarbonate was added and the mixture was extracted with ethyl acetate. The extract was washed with water, dried over anhydrous magnesium sulfate and filtered. After evaporating the solvent, the obtained residue was subjected to silica gel column chromatography to give 3.7 g (84%) of the title compound as an oily substance.
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-5d5a9bdc3c81411cb148de996528a9c6 |
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| Quellennotiz | uspto-grants-2006_08 |
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