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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Penten-3-oneHCID 15394—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt2-Butyl-4-chloro-5-methoxy-1-indanoneHCID 21990917—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-Butyl-4-chloro-5-methoxy-2-(3-oxopentyl)-1-indanoneHCID 2199091193,9%

Reaktionsbedingungen

Temperatur60 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087599B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-d1cb4b3435da4997860140228da64a57
Quellennotizuspto-grants-2006_08