HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2073310Erstellt: 25. Oktober 2026
N-[1,1-dimethyl(3-pyridyl)butyl]-2-nitrobenzeneacetamide → alpha,alpha-Dimethyl-3-pyridinebutanamine
https://huagongshe.com/reaction/2073310
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N-[1,1-dimethyl(3-pyridyl)butyl]-2-nitrobenzeneacetamide | HCID 14347488 | — |
| Edukt | HCID 178418361 | HCID 178418361 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | alpha,alpha-Dimethyl-3-pyridinebutanamine | HCID 14547286 | 77,8% |
Reaktionsschritte
A solution of 35.2 g of N-[1.1-dimethyl-4-(3-pyridyl) butyl]-2-nitrobenzeneacetamide in 250 mL of acetic acid was hydrogenated over 3.5 g of 10% Pd/C at atmospheric Pressure and ambient temperature. The reaction was exothermic and stopped abruptly after the uptake of the theoretical amount of hydrogen (7.5 L). The catalyst was removed by filtration and the filtrate was heated at reflux for 90 minutes. After the solution was cooled. 10 mL of conc. HCl was added and the solvent was removed under reduced pressure. The residue was taken up in IL of water and extracted with ethyl acetate (4×200 mL) to remove the by product, oxindole. The aqueous layer was basified with 10N NaOH and extracted with dichloromethane to give. after evaporation of the dried (K2CO3) extracts 15 g of product. The material was distilled on a Kugelrohr apparatus (95° C; 0.1 mm) to yield 14.3 g of alpha,alphadimethyl-3-pyridinebutanamine.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04916145 |
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| Quelldatensatz | uspto-grants-1990_04 |
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| ORD ID | ord-a8f5e68d62344dd7b2f30288b5e05637 |
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| Quellennotiz | uspto-grants-1990_04 |
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