HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40182Erstellt: 23. Oktober 2026
Tetrahydrofuran → Ethyl 3-(7-methoxyquinolin-4-yl)propanoate
https://huagongshe.com/de/reaction/40182
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Tri-tert-butylphosphine tetrafluoroborate | HCID 2734635 | — |
| Edukt | 4-Chloro-7-methoxyquinoline | HCID 10607829 | — |
| Edukt | HCID 178471816 | HCID 178471816 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | Ammonium Hydroxide | HCID 14923 | — |
| Produkt | Ethyl 3-(7-methoxyquinolin-4-yl)propanoate | HCID 67503802 | — |
Reaktionsschritte
4-chloro-7-methoxyquinoline (0.35 g, 2 mmol), tri-t-butylphosphonium tetrafluoroborate (0.05 g, 0.2 mmol), and tris(dibenzylideneacetone)dipalladium (0) (0.08 g, 0.09 mmol) were combined. The reaction vessel was purged and flushed with nitrogen three times, followed by addition of 3-ethoxy-3-oxopropylzinc bromide in THF (10 mL, 5 mmol, 0.5 M). The reaction mixture was microwaved at 150° C. for 60 minutes. Upon completion, ammonium hydroxide (10 mL) was added. After 30 minutes the mixture was filtered and the filtrate was partitioned between water and ethyl acetate. Extracted with ethyl acetate (3×20 mL). The organic layers were combined, washed with brine, dried over magnesium sulfate, and concentrated. Purified by MPLC with a gradient of 20 to 50% EtOAc in CH2Cl2. (ESI, pos. ion) m/z: 354.1 (M+H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524900B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-2749dc371527437e9924f4eb2acea80b |
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| Quellennotiz | uspto-grants-2013_09 |
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