HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7851Erstellt: 23. Oktober 2026
1-Penten-3-one → 2-Butyl-5-methoxy-4-methyl-2-(3-oxopentyl)-1-indanone
https://huagongshe.com/de/reaction/7851
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Penten-3-one | HCID 15394 | — |
| Edukt | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Edukt | 2-Butyl-5-methoxy-4-methyl-1-indanone | HCID 21990883 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-Butyl-5-methoxy-4-methyl-2-(3-oxopentyl)-1-indanone | HCID 21990930 | — |
Reaktionsschritte
A solution of 2-butyl-5-methoxy-4-methyl-1-indanone (100 mg, 0.43 mmol) in tetrahydrofuran (0.43 mL) was treated with ethyl vinyl ketone (EVK, 0.064 mL, 0.646 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU, 0.013 mL, 0.086 mmol). The resulting solution was stirred under a nitrogen atmosphere and heated in an oil bath at 60° C. After 24 hour, more EVK (0.064 mL) and DBU (0.013 mL) were added and the solution was heated an additional 24 hours at 60° C. The reaction mixture was diluted with EtOAc (10 mL) and washed with water (10 mL) containing 2N HCl (1 mL). The organic phase was washed with brine (5 mL), dried over MgSO4, filtered, and evaporated under vacuum to provide crude 2-butyl-5-methoxy-4-methyl-2-(3-oxopentyl)-1-indanone.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07087599B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-ab9cbb76965644d483935f81bfcf3531 |
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| Quellennotiz | uspto-grants-2006_08 |
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