HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44689Erstellt: 23. Oktober 2026
Ethyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylate → Ethyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate
https://huagongshe.com/de/reaction/44689
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Ethyl 4-hydroxy-4-(nitromethyl)-1-piperidinecarboxylate | HCID 22708806 | — |
| Katalysator | Palladium hydroxide | HCID 9942167 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Ethyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate | HCID 14049029 | — |
Reaktionsschritte
A mixture of ethyl 4-hydroxy-4-(nitromethyl)piperidine-1-carboxylate (5.2 g, 22.4 mmol) and 20% palladium hydroxide on carbon (0.50 g) in ethanol (190 mL) was hydrogenated at 35 psi (2.4×105 Pa) on a Parr apparatus for 5 h. The mixture was filtered through CELITE filter agent and the filtrate was concentrated. By 1H NMR analysis, the reaction was incomplete and the crude material was subjected to the reaction conditions again with fresh 20% palladium hydroxide on carbon (0.50 g) for another 24 h. The mixture was filtered through CELITE filter agent and the filtrate was concentrated to provide ethyl 4-(aminomethyl)-4-hydroxypiperidine-1-carboxylate, which was concentrated from chloroform to remove residual ethanol before using in the next reaction.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08541438B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-e97a7697d026407fb91118f4daf04744 |
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| Quellennotiz | uspto-grants-2013_09 |
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