HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22228Erstellt: 23. Oktober 2026
1,3-Propanediamine → N-(5-trifluoromethyl-2-pyridylmethyl)trimethylenediamine
https://huagongshe.com/de/reaction/22228
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,3-Propanediamine | HCID 428 | — |
| Edukt | 5-(Trifluoromethyl)pyridine-2-carbaldehyde | HCID 14422792 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | N-(5-trifluoromethyl-2-pyridylmethyl)trimethylenediamine | HCID 14207162 | 75,1% |
Reaktionsschritte
5-Trifluoromethylpicoline aldehyde (3.5 g) was added dropwise at room temperature to a solution of trimethylenediamine (7.4 g) in benzene (70 ml). After the addition, the mixture was gradually heated with stirring, and then while separating water as an azeotrope, refluxed for 2 hours. Benzene was distilled off under reduced pressure, and then the residue was dissolved in ethanol (100 ml). With stirring at 10° to 15° C., sodium borohydride (0.9 g) was added little by little. The mixture was then stirred at room temperature for 2 hours. Ethanol was distilled off at less than 30° C. Dichloromethane was added to the residue, and a portion of it soluble in dichloromethane was separated. Dichloromethane was distilled off under reduced pressure, and volatile materials were removed at 1 mmHg and less than 60° C. to give N-(5-trifluoromethyl-2-pyridylmethyl)trimethylenediamine (3.5 g) as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05428032 |
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| Quelldatensatz | uspto-grants-1995_06 |
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| ORD ID | ord-196a48b2d40b41e897ee47e90e526120 |
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| Quellennotiz | uspto-grants-1995_06 |
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