HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64575Erstellt: 24. Oktober 2026
Sodium Chloride → Propanoic acid, 2-(4-((6,7-dichloro-2-quinoxalinyl)oxy)phenoxy)-, methyl ester
https://huagongshe.com/de/reaction/64575
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Chloride | HCID 5234 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Propanoic acid, 2-(4-hydroxyphenoxy)-, methyl ester | HCID 366926 | — |
| Edukt | 2,6,7-Trichloroquinoxaline | HCID 10036978 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Propanoic acid, 2-(4-((6,7-dichloro-2-quinoxalinyl)oxy)phenoxy)-, methyl ester | HCID 187100 | — |
Reaktionsschritte
In a nitrogen atmosphere, a solution of 3.9 g (0.02 mole) methyl 2-(4-hydroxyphenoxy)propanoate in 20 cc of dimethylformamide was added dropwise at about 15° C. to a suspension of 0.8 g sodium hydride in 10 cc dimethylformamide. When the evolution of hydrogen ceased, 4.7 g of (0.02 mole) 2,6,7-trichloroquinoxaline was added and the reaction mixture was heated for 5 hours at ~130° C. Filtering the reaction mixture yielded a small amount of insoluble material. The filtrate was poured into approximately 200 cc of ice-water. Sodium chloride was added to the solution which was then extracted with 1200 cc of ether (4×300). The ethereal extracts were combined and dried over magnesium sulfate. The ether was removed under vacuum and the crude product was crystallized from CH3OH. Yield 2.8 g, m.p. 100°-105°.
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-838dd883dd6b4c7281091294dd3bc776 |
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| Quellennotiz | uspto-grants-1986_09 |
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