Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7831Erstellt: 23. Oktober 2026

Butanal → 2-Butyl-5-methoxy-1-indanone

https://huagongshe.com/de/reaction/7831

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButanalHCID 261—
EduktHydrochloric AcidHCID 313—
EduktPotassium HydroxideHCID 14797—
Edukt5-Methoxyindan-1-oneHCID 78787—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthanolHCID 702—
Produkt2-Butyl-5-methoxy-1-indanoneHCID 1204575253,2%

Reaktionsschritte

A mixture of 5-methoxy-1-indanone (25.0 g, 154 mmol), 85% KOH (2.03 g, 30.8 mmol), 10% palladium on activated carbon (2 g), and ethanol (150 mL) was placed under a hydrogen atmosphere and stirred while butyraldehyde (16.7 mL, 185 mmol) was added over 2 minutes. The mixture warmed during the addition. The resulting mixture was hydrogenated at room temperature for 3 hours, then filtered to remove the catalyst. The filtrate was acidified with 2N HCl (15.4 mL, 30.8 mmol) and evaporated under vacuum. The residue was partitioned between EtOAc (500 mL) and water (500 mL). The organic phase was washed with water (500 mL) and brine (100 mL), dried over MgSO4, filtered, and evaporated under vacuum to an oil (33.5 g). The crude product was purified by column chromatography on EM silica gel 60 (230-400 mesh, 670 g), eluting first with CH2Cl2 and then with 5% EtOAc in CH2Cl2, to afford 2-butyl-5-methoxy-1-indanone (17.9 g) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087599B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-81064133f67440459d71cf2f2f14c79e
Quellennotizuspto-grants-2006_08