関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzoyl Peroxide | HCID 7187 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | 6-Methylquinoxaline | HCID 242567 | — |
| 反応物 | 6-(Bromomethyl)quinoxaline | HCID 10214510 | — |
| 溶媒 | Chlorobenzene | HCID 7964 | — |
| 溶媒 | Pentane | HCID 8003 | — |
| 溶媒 | Butylamine | HCID 8007 | — |
| 生成物 | N-(Quinoxalin-6-ylmethyl)butan-1-amine | HCID 12071593 | — |
反応手順
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).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06750343B2 |
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| 出典データセット | uspto-grants-2004_06 |
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| ORD ID | ord-6bd3ee9d2695469e9d5b114ef71ea79d |
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| 出典メモ | uspto-grants-2004_06 |
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