HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 221849Erstellt: 24. Oktober 2026
1-(4-Methoxyphenyl)butane-1,3-dione → 4-(4-Methoxybenzoyl)-5-methylisoxazole-3-carboxylic acid ethyl ester
https://huagongshe.com/de/reaction/221849
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-(4-Methoxyphenyl)butane-1,3-dione | HCID 77640 | — |
| Edukt | Sodium ethoxide | HCID 2723922 | — |
| Edukt | Ethyl chloro(hydroximino)acetate | HCID 6816376 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 4-(4-Methoxybenzoyl)-5-methylisoxazole-3-carboxylic acid ethyl ester | HCID 59652027 | — |
Reaktionsschritte
To 7.04 mL of 21% sodium ethoxide in ethanol (18.8 mmol) in 60 mL ethanol at 0° C. was added 4.70 g of 1-(4-methoxyphenyl)butane-1,3-dione (17.1 mmol) in 60 mL ethanol dropwise over 24 minutes. After 30 min a solution of 2.59 g of ethyl chloro-(hydroximino)acetate (17.1 mmol) in 30 mL ethanol was added dropwise over 6 minutes. The reaction was warmed to room temperature slowly. When TLC indicated the reaction was complete, the reaction was concentrated in vacuo. Water and saturated NaHCO3 was added and the product extracted with ethyl acetate. The ethyl acetate extracts were dried with Na2SO4, filtered, and concentrated in vacuo. The crude material was purified via silica gel chromatography eluting with 8:1 hexane:ethyl acetate to give 4-(4-methoxybenzoyl)-5-methylisoxazole-3-carboxylic acid ethyl ester which was dried overnight under high vacuum to give 3.74 g (71.8%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08207168B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-61dc1495a4384999961add7a19d8179b |
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| Quellennotiz | uspto-grants-2012_06 |
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