HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 745Erstellt: 23. Oktober 2026
Ethyl 4-piperidinecarboxylate → Ethyl 1-(4-(tert-butoxycarbonyl)phenyl)piperidine-4-carboxylate
https://huagongshe.com/de/reaction/745
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl 4-piperidinecarboxylate | HCID 70770 | — |
| Edukt | Tert-butyl 4-bromobenzoate | HCID 11334366 | — |
| Reagenz | Cesium carbonate | HCID 10796 | — |
| Katalysator | Binap, (A+-)- | HCID 634876 | — |
| Katalysator | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | Ethyl 1-(4-(tert-butoxycarbonyl)phenyl)piperidine-4-carboxylate | HCID 19063865 | 0% |
Reaktionsschritte
1\. To a microwave tube was added tert-butyl 4-bromobenzoate (1.328 g, 5.16 mmol), ethyl piperidine-4-carboxylate (1.000 g, 5.16 mmol), Cs2CO3 (5.05 g, 15.49 mmol), Pd2dba3 (0.473 g, 0.52 mmol), and BINAP (0.643 g, 1.03 mmol). The mixture was dissolved in [Solvents] and sealed. The tube was de-gassed and inflated with N2. 2\. The reaction was heated at 110°C in oil-bath overnight. LCMS showed reaction complete. The reaction mixture was filter through celite pad and the solution was loaded to column for a ISCO purification (30% EtOAc in Hex). The purification is difficult with multiple by-products. Several ISCO purification was carried out and fractions were combined with other batches. Yield was poor.
Herkunft & Nachweise
| Quelldatensatz | 750 AstraZeneca ELN dataset |
|---|
| ORD ID | ord-1beac9199051463f81c658e8f7cb9a0d |
|---|
| Quellennotiz | 750 AstraZeneca ELN dataset |
|---|