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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7828Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/7828

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButanalHCID 261—
EduktDiisopropylamineHCID 7912—
EduktPentaneHCID 8003—
Edukt5-Methoxyindan-1-oneHCID 78787—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Butylidene-5-methoxy-1-indanoneHCID 67402813—

Reaktionsschritte

A solution of diisopropylamine (0.227 mL, 1.62 mmol) in anhydrous tetrahydrofuran (THF, 15 mL) was placed under a nitrogen atmosphere, cooled in an ice bath, and stirred while a 2.0M solution of butyllithium in pentane (0.771 mL, 1.54 mmol) was added dropwise over 2 minutes. The solution was stirred at room temperature for 15 minutes, then cooled in a dry ice-acetone bath and treated dropwise over 3 minutes with a solution of 5-methoxy-1-indanone (250 mg, 1.54 mmol) in THF (2 mL). After stirring at −78° C. for 20 minutes, the reaction mixture was treated with butyraldehyde (0.167 mL, 1.85 mmol). After stirring an additional 26 minutes at −78° C., the reaction mixture was removed from the cooling bath and stirred at room temperature for 90 hours. The reaction mixture was treated with saturated aqueous NH4Cl solution (10 mL) and extracted with EtOAc (15 mL). The organic phase was washed with brine (25 ml), dried over MgSO4, filtered, and evaporated under vacuum to an oil (353 mg). The crude product was purified by silica gel chromatography on a Biotage FLASH 12M column (1.2×15 cm), eluting with 7:1 hexanes-EtOAc, to afford 2-butylidene-5-methoxy-1-indanone (205 mg) as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07087599B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-348e8a54c7c84684b360fbaec8b6e185
Quellennotizuspto-grants-2006_08