HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 220481Erstellt: 25. Oktober 2026
Sodium hydride → 1-(3,5-Dimethylisoxazol-4-ylmethyl)-1H-pyrazole-4-carbaldehyde
https://huagongshe.com/reaction/220481
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Isoxazole, 4-(chloromethyl)-3,5-dimethyl- | HCID 88246 | — |
| Edukt | 1H-pyrazole-4-carbaldehyde | HCID 5130673 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-(3,5-Dimethylisoxazol-4-ylmethyl)-1H-pyrazole-4-carbaldehyde | HCID 86641653 | — |
Reaktionsschritte
Add N,N-dimethylformamide (3 mL) to sodium hydride (0.092 g, 2.29 mmol) and stir at 0° C. Add 1-H-pyrazole-4-carboxaldehyde (0.200 g, 2.08 mmol) and stir at 0° C. for 20 min. Dissolve 4-chloromethyl-3,5-dimethylisoxazole (0.318 g, 2.18 mmol) in N,N-dimethylformamide (4 mL) and add to reaction mixture. Stir reaction at room temperature for 18 hr. Quench with aqueous saturated sodium bicarbonate solution. Add ethyl acetate and separate organic layer. Extract aqueous layer twice with ethyl acetate. Dry combined organic layers (magnesium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 25:75 to 75:25 ethyl acetate:hexanes), to give the title preparation (387 mg, 91%). GC-MS: m/z=205 [M+].
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08202873B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-b49960dd7d97476f83026d6423df702e |
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| Quellennotiz | uspto-grants-2012_06 |
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