HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 54421Erstellt: 25. Oktober 2026
3,5-Dimethylisoxazole → 2-(3-Methyl-isoxazol-5-yl)-1-(2-tert.butyldimethylsiloxy-phenyl)-ethanone
https://huagongshe.com/reaction/54421
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3,5-Dimethylisoxazole | HCID 9312 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Methyl 2-tert.butyldimethylsiloxybenzoate | HCID 131719984 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | 2-(3-Methyl-isoxazol-5-yl)-1-(2-tert.butyldimethylsiloxy-phenyl)-ethanone | HCID 131719983 | 50,4% |
Reaktionsschritte
52 ml of 1N solution of n-butyllithium in hexane were added to a solution of 6 g of 3,5-dimethylisoxazol in 200 ml of tetrahydrofuran at -78° C. After stirring for 1 h 15 g of methyl 2-tert.butyldimethylsiloxybenzoate in 50 ml of tetrahydrofuran were added at the same temperature. The reaction mixture was slowly warmed up to -20° C. A saturated aqueous solution of ammonium chloride was added, the mixture was extracted several times with ethylacetate. The organic phase was separated, washed with water and dried over magnesium sulfate. Chromatography on silica gel with heptane/ethylacetate gave 9.4 g of the product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05622953 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-a7602e0c89e6449eacff8936f61394cd |
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| Quellennotiz | uspto-grants-1997_04 |
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