HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 554140Erstellt: 24. Oktober 2026
3-Pyridinecarboxaldehyde → 5-Oxo-1-(3-pyridinylmethyl)proline
https://huagongshe.com/de/reaction/554140
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | D-Glutamic Acid | HCID 23327 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 5-Oxo-1-(3-pyridinylmethyl)proline | HCID 10536887 | 61,8% |
Reaktionsschritte
D-glutamic acid (2.21 g, 15 mmol) was dissolved in 2N aqueous sodium hydroxide (15 ml, 30 mmol) at 0° C. and then treated with pyridine-3-carboxaldehyde (1.41 ml, 15 mmol) in ethanol (3 ml). The mixture was stirred at room temperature for 30 minutes and then cooled to 0° C. and treated portion-wise with sodium borohydride (0.189 g, 5 mmol). The mixture was allowed to warm to room temperature with stirring over 4 hrs then after washing with diethyl ether it was acidified to pH5-6 using concentrated hydrochloric acid. The resulting precipitate was collected by filtration, washed with diethyl ether, and dried in vacuo. This material was then taken up in ethanol (50 ml) and refluxed overnight. Fine solids were removed by filtration and then concentration gave 5-oxo-1-(3-pyridinylmethyl)proline (2.04 g) as a white solid which was used without any further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08048907B2 |
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| Quelldatensatz | uspto-grants-2011_11 |
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| ORD ID | ord-753fcc2df7464fd19953f6b1a095e7f5 |
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| Quellennotiz | uspto-grants-2011_11 |
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