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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | 1-Bromo-3,4-(methylenedioxy)benzene | HCID 75831 | — |
| Edukt | Lithium diisopropylamide | HCID 2724682 | — |
| Edukt | Isoquinoline-5-carboxaldehyde | HCID 7016853 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | alpha-(5-BRomo-1,3-benzodioxol-4-yl)-5-isoquinolinemethanol | HCID 10981200 | 65% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07091212B2 |
|---|
| Quelldatensatz | uspto-grants-2006_08 |
|---|
| ORD ID | ord-d7ba93572fa64fddbb46271e8f729e27 |
|---|
| Quellennotiz | uspto-grants-2006_08 |
|---|