HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64583Erstellt: 24. Oktober 2026
Dimethylformamide → Methyl 4-[4-(3-methyl-3-quinoxalinyloxy)phenoxy]pent-2-enoate
https://huagongshe.com/de/reaction/64583
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 2-(4-Hydroxyphenoxy)-3-methylquinoxaline | HCID 13670538 | — |
| Edukt | Methyl 4-bromo-2-pentenoate | HCID 54128087 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Methyl 4-[4-(3-methyl-3-quinoxalinyloxy)phenoxy]pent-2-enoate | HCID 70469256 | — |
Reaktionsschritte
In a nitrogen atmosphere, add a solution of 5.4 g (0.02 mole) 2-(4-hydroxyphenoxy)-3-methylquinoxaline in 30 cc dimethylformamide to 0.9 g (0.02 mole) 57% sodium hydride in 20 cc dimethylformamide at about 20° C. When the evolution of hydrogen ceases, add 3.9 g (0.02 mole) methyl 4-bromo-2-pentenoate. Heat the reaction mixture at approximately 80° C. until the reaction is complete. Pour the reaction mixture into water and extract with ether. Combine the ethereal extracts and dry over magnesium sulfate. Removal of the ether gives the desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04609396 |
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| Quelldatensatz | uspto-grants-1986_09 |
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| ORD ID | ord-aa9f6b8071fc48d085f88192195dc687 |
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| Quellennotiz | uspto-grants-1986_09 |
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