HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1589201Erstellt: 25. Oktober 2026
Benzaldehyde → N-[2-(benzylamino)ethyl]pyridine-3-carboxamide
https://huagongshe.com/reaction/1589201
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzaldehyde | HCID 240 | — |
| Edukt | SG 1842 | HCID 571799 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | N-[2-(benzylamino)ethyl]pyridine-3-carboxamide | HCID 4242394 | — |
Reaktionsschritte
A solution of N-(2-aminoethyl)pyridine-3-carboxamide (26.5 g.) and benzaldehyde (16.35 ml.) in ethanol (220 ml.) was kept for 48 hours. A small quantity of solid was removed by filtration. Sodium borohydride (6.1 g.) was then added to the filtrate which was stirred for 1 hour. Glacial acetic acid was then added cautiously until the solution was neutral. The solution was diluted with water (100 ml.) and basified with 2M sodium hydroxide. The mixture was extracted with ethyl acetate (3×200 ml.) and the extracts washed with saturated brine, dried (Na2SO4) and evaporated. The residue was purified by chromatography on a column of Florisil (200 g.), eluting with ethyl acetate, to yield N-[2-(benzylamino)ethyl]pyridine-3-carboxamide (29.5 g.) as a pale brown oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04568691 |
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| Quelldatensatz | uspto-grants-1986_02 |
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| ORD ID | ord-7a9c8347d88d4f9090754c71dd962048 |
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| Quellennotiz | uspto-grants-1986_02 |
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