Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,3-Propanediamine | HCID 428 | — |
| Edukt | Benzamide | HCID 2331 | — |
| Produkt | n-(3-Aminopropyl)benzamide | HCID 238993 | 33,4% |
Reaktionsschritte
Benzamide (25 g, 0.20 mol) and 1,3-diaminopropane (45.9 g, 0.60 mol) were combined in a Parr vessel and heated to 150° C. for 15 hours. The vessel was cooled and the reaction mixture was concentrated under vacuum to remove excess diamine. The residue was dissolved in water (500 mL) and concentrated hydrochloric acid was added to adjust the pH to <1. The resulting precipitate (starting benzamide and diacylated product) was removed by filtration. The filtrate was washed with dichloromethane. The aqueous layer was made strongly basic by the addition of 50% sodium hydroxide and then it was extracted with dichloromethane (4×300 mL). The extracts were combined, washed with brine (300 mL), dried over sodium sulfate and then concentrated under vacuum to provide 11.9 g of N-(3-aminopropyl)benzamide as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06756382B2 |
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| Quelldatensatz | uspto-grants-2004_06 |
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| ORD ID | ord-4b0fa44ee2b241e295a9ce7801e17bdd |
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| Quellennotiz | uspto-grants-2004_06 |
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