HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2242948Erstellt: 25. Oktober 2026
Acetic Acid → [1-(3-Ethoxy-4-methoxy-benzyl)-piperidin-4-yl]-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/2242948
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | 3-Ethoxy-4-methoxybenzaldehyde | HCID 244728 | — |
| Edukt | 4-(N-Boc-amino)piperidine | HCID 723833 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | [1-(3-Ethoxy-4-methoxy-benzyl)-piperidin-4-yl]-carbamic acid tert-butyl ester | HCID 67147361 | 53% |
Reaktionsschritte
A mixture of piperidin-4-yl-carbamic acid tert-butyl ester (10.0 g, 50.0 mmol, 1.0 equiv), 3-ethoxy-4-methoxy-benzaldehyde (10.8 g, 60.0 mmol, 1.2 equiv; commercially available) and acetic acid (11.4 mL, 12.01 g, 200.0 mmol, 4.0 equiv) in ethanol (40 mL) was heated by microwave irradiation to 100° C. for 5 min. Sodium cyanoborohydride (6.27 g, 100.0 mmol, 2.0 equiv), dissolved in ethanol (20 mL), was added and the reaction mixture heated by microwave irradiation to 100° C. for an additional time period of 5 min. The solvent was removed under reduced pressure and the crude reaction product extracted from a solution of 1 M NaOH (200 mL) with ethyl acetate (3×100 mL). The combined organic phases were dried over MgSO4, concentrated by evaporation under reduced pressure and the crude material purified with column chromatography on silica eluting with ethyl acetate to yield 9.71 g (53%) of the title compound as a white solid. MS (ISP): 365.3 [M+H]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07674804B2 |
|---|
| Quelldatensatz | uspto-grants-2010_03 |
|---|
| ORD ID | ord-89c5b060abfb4b89a658be4d2b1d78f9 |
|---|
| Quellennotiz | uspto-grants-2010_03 |
|---|