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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8711Erstellt: 23. Oktober 2026

Ethyl Acetate → alpha-(5-BRomo-1,3-benzodioxol-4-yl)-5-isoquinolinemethanol

https://huagongshe.com/de/reaction/8711

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
Edukt1-Bromo-3,4-(methylenedioxy)benzeneHCID 75831—
EduktLithium diisopropylamideHCID 2724682—
EduktIsoquinoline-5-carboxaldehydeHCID 7016853—
LösungsmittelTetrahydrofuranHCID 8028—
Produktalpha-(5-BRomo-1,3-benzodioxol-4-yl)-5-isoquinolinemethanolHCID 1098120065%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of 4-bromo-1,2-(methylendioxy)benzene (3.01 g, 15 mmol) in THF (20 mL) at −78° C. was added dropwise lithium diisopropylamide (10.6 mL of 1.5 M in cyclohexane, 16 mmol). The reaction mixture was stirred at −78° C. under argon for 20 minutes. A brown solution was formed. A solution of 5-isoquinolinecarboxaldehyde (1.90 g, 12 mmol) in THF (4 mL) was added dropwise. The resulting mixture was stirred at −78° C. for 10 minutes and warmed to room temperature. Stirring was continued for 30 minutes at room temperature, and then the mixture was quenched with saturated NH4Cl solution. The product was extracted with EtOAc and the solvent was removed under reduced pressure. Chromatography (SiO2 Type-H, 35% EtOAc in Hexanes) of the residue yielded the title compound as a yellow solid (2.8 g, 7.8 mmol, 65% yield): mp 173–175° C.;

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091212B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-d7ba93572fa64fddbb46271e8f729e27
Quellennotizuspto-grants-2006_08