Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzoyl Peroxide | HCID 7187 | — |
| Edukt | N-bromobutanimide | HCID 67184 | — |
| Edukt | 6-Methylquinoxaline | HCID 242567 | — |
| Edukt | 6-(Bromomethyl)quinoxaline | HCID 10214510 | — |
| Lösungsmittel | Chlorobenzene | HCID 7964 | — |
| Lösungsmittel | Pentane | HCID 8003 | — |
| Lösungsmittel | Butylamine | HCID 8007 | — |
| Produkt | N-(Quinoxalin-6-ylmethyl)butan-1-amine | HCID 12071593 | — |
Reaktionsschritte
In a 50 ml flask, 6-methyl-quinoxaline (1.25 g, 8.68 mmol) was dissolved together with N-bromosuccinimide (2.32 g, 13.0 mmol) and benzoyl-peroxide (0.15 g, 0.62 mmol) in 31. g of chlorobenzene. The solution was stirred with heating at 85° C. for 2.0 hours to yield a reddish solution. The solution was cooled down to room temperature and one volume of pentane was added to facilitate the removal of succinimides. The precipitate was washed with pentane and the extracts were combined with the chlorobenzene solution. The yellow solution was vacuum dried to give a yellow residue mainly composed of 6-bromomethyl-quinoxaline. The yellow solid was dissolved in 19.0 g of n-butylamine to give a yellow solution that was stirred at room temperature for ˜5 minutes. Analysis of a sample showed that the 6-bromomethyl-quinoxaline was consumed to give exclusively 6-n-butylaminomethyl-quinoxaline as a deep yellow oil (1.71 g, 92% over all yield). MS (70 ev): 215 M+, 172 (M+—CH3—CH2—CH2),143 (M+—CH3—CH2—CH2—CH2).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06750343B2 |
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| Quelldatensatz | uspto-grants-2004_06 |
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| ORD ID | ord-6bd3ee9d2695469e9d5b114ef71ea79d |
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| Quellennotiz | uspto-grants-2004_06 |
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