HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 484Erstellt: 23. Oktober 2026
1,2,3,4-Tetrahydroisoquinoline → methyl 4-(3,4-dihydro-1H-isoquinolin-2-yl)benzoate
https://huagongshe.com/de/reaction/484
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,2,3,4-Tetrahydroisoquinoline | HCID 7046 | — |
| Edukt | Methyl 4-bromobenzoate | HCID 12081 | — |
| Reagenz | Cesium carbonate | HCID 10796 | — |
| Katalysator | Binap, (A+-)- | HCID 634876 | — |
| Katalysator | Palladium (II) acetate | HCID 4144353 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | methyl 4-(3,4-dihydro-1H-isoquinolin-2-yl)benzoate | HCID 57327469 | 0% |
Reaktionsschritte
methyl 4-bromobenzoate (100 mg, 0.47 mmol), [Reactants] and Cesium carbonate (152 mg, 0.47 mmol) were mixed in toluene (4 mL) and degassed by bubbling nitrogen through solution. Palladium acetate (5.22 mg, 0.02 mmol) and rac-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl (20.27 mg, 0.03 mmol) were added and the vial was capped and heated at 100°C over 5 days. Product had formed in mixture. Workup by dilution with EtOAc, washing with water, then extraction with 2M HCl. The HCl extract was neutralized with 2M NaOH and extracted with EtOAc and the EtOAc phase was dried (K2CO3) and evaporated to give the crude product. No product. Discarded.
Herkunft & Nachweise
| Quelldatensatz | 750 AstraZeneca ELN dataset |
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| ORD ID | ord-d7ba527a2d2d4d7591368f0e50bee26a |
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| Quellennotiz | 750 AstraZeneca ELN dataset |
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