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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8711Generated: October 26, 2026

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

https://huagongshe.com/reaction/8711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1-Bromo-3,4-(methylenedioxy)benzeneHCID 75831—
ReactantLithium diisopropylamideHCID 2724682—
ReactantIsoquinoline-5-carboxaldehydeHCID 7016853—
SolventTetrahydrofuranHCID 8028—
Productalpha-(5-BRomo-1,3-benzodioxol-4-yl)-5-isoquinolinemethanolHCID 1098120065%

Reaction Conditions

Temperature-78 °C

Reaction Steps

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.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091212B2
Source datasetuspto-grants-2006_08
ORD IDord-d7ba93572fa64fddbb46271e8f729e27
Source noteuspto-grants-2006_08