HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 573563Erstellt: 24. Oktober 2026
Dichloromethane → Ethyl 2-cyano-3-[3-(methyloxy)phenyl]-2-butenoate
https://huagongshe.com/de/reaction/573563
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | Ethyl cyanoacetate | HCID 7764 | — |
| Edukt | 3-Methoxyacetophenone | HCID 11460 | — |
| Edukt | Hexamethyldisilazane | HCID 13838 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Ethyl 2-cyano-3-[3-(methyloxy)phenyl]-2-butenoate | HCID 4115002 | 86,3% |
Reaktionsschritte
Hexamethyldisilazane (17.45 mL, 83 mmol) was added dropwise to acetic acid (38.1 mL, 666 mmol) (caution exothermic, maintain below 70° C.) stirred under an atmosphere of nitrogen. The resulting mixture was added to a solution of 1-[3-(methyloxy)phenyl]ethanone (9.14 mL, 66.6 mmol) and ethyl cyanoacetate (11.75 mL, 110 mmol) in acetic acid (16 mL), which was then stirred at 70° C. for 18 h. The mixture was then allowed to cool to RT and DCM (350 mL) and water (125 mL) were added. The organic layer was then separated and washed with additional water (125 mL) and dried with anhydrous MgSO4, filtered and evaporated to dryness. The residue was purified on silica, eluting with a gradient of 0-30% ethyl acetate in isohexane and further purified on silica, eluting with a gradient of 0-25% ethyl acetate in isohexane, to afford the title compound (14.1 g). LCMS (A) m/z: 246 [M+1]+, Rt 1.28 min (basic).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09029545B2 |
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| Quelldatensatz | uspto-grants-2015_05 |
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| ORD ID | ord-02851e9ff45a4b3ca21cb5998be3404f |
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| Quellennotiz | uspto-grants-2015_05 |
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