HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1795026Erstellt: 27. Oktober 2026
Sodium borohydride → (5-(4-(Trifluoromethyl)phenyl)-4,5-dihydroisoxazol-3-yl)methanol
https://huagongshe.com/reaction/1795026
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | Ethyl 5-(4-(trifluoromethyl)phenyl)-4,5-dihydroisoxazole-3-carboxylate | HCID 22064077 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | (5-(4-(Trifluoromethyl)phenyl)-4,5-dihydroisoxazol-3-yl)methanol | HCID 22184760 | 78% |
Reaktionsschritte
To a stirred mixture of sodium borohydride (378 mg, 10.0 mmol) in ethanol (20 ml) was added slowly a solution of ethyl 5-(4-(trifluoromethyl)phenyl)-4,5-dihydroisoxazole-3-carboxylate (1.6 g, 5.75 mmol) in ethanol (10 mL). The resulting reaction mixture was stirred under an atmosphere of nitrogen for 8 hours. Ethanol was removed under reduced pressure and water (20 ml) added. The aqueous mixture was acidified to about pH 3 with concentrated HCl, and the acidic solution extracted with ethyl acetate (3×20 ml). The resulting organic phase was washed with saturated aqueous sodium bicarbonate (20 ml), 30% aqueous ammonium chloride(20 ml), brine, dried over sodium-sulfate, concentrated, and purified using chromatography (3% MeOH in CH2Cl2) to afford (5-(4-(trifluoromethyl)phenyl)-4,5-dihydroisoxazol-3-yl)methanol (1.1 g, M+1=246.1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07026321B2 |
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| Quelldatensatz | uspto-grants-2006_04 |
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| ORD ID | ord-462b83e0aa924d4bb79f599a9119fbea |
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| Quellennotiz | uspto-grants-2006_04 |
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