HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7855Erstellt: 23. Oktober 2026
1-Penten-3-one → 2-Butyl-4-chloro-5-methoxy-2-(3-oxopentyl)-1-indanone
https://huagongshe.com/de/reaction/7855
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-4-chloro-5-methoxy-1-indanone | HCID 21990917 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-Butyl-4-chloro-5-methoxy-2-(3-oxopentyl)-1-indanone | HCID 21990911 | 93,9% |
Reaktionsschritte
A solution of 2-butyl-4-chloro-5-methoxy-1-indanone (200 mg, 0.79 mmol) in anhydrous tetrahydrofuran (0.8 mL) was placed under a nitrogen atmosphere and treated with ethyl vinyl ketone (0.118 mL, 1.19 mmol) followed by 1,8-diazabicyclo[5.4.0]undec-7-ene (0.024 mL, 0.158 mmol). The resulting solution was stirred and heated in an oil bath at 60° C. for 47 hours. After cooling to room temperature, the reaction mixture was diluted with EtOAc (20 mL) and washed with water (20 mL) containing 2N HCl (2 mL). The organic phase was washed with brine (10 mL), dried over MgSO4, filtered, and evaporated under vacuum to provide crude 2-butyl-4-chloro-5-methoxy-2-(3-oxopentyl)-1-indanone (250 mg) as an oil.
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-d1cb4b3435da4997860140228da64a57 |
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| Quellennotiz | uspto-grants-2006_08 |
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