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HRID 353323作成日:2026年10月26日

Benzoyl Peroxide → N-(Quinoxalin-6-ylmethyl)butan-1-amine

https://huagongshe.com/reaction/353323

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl PeroxideHCID 7187—
反応物N-bromobutanimideHCID 67184—
反応物6-MethylquinoxalineHCID 242567—
反応物6-(Bromomethyl)quinoxalineHCID 10214510—
溶媒ChlorobenzeneHCID 7964—
溶媒PentaneHCID 8003—
溶媒ButylamineHCID 8007—
生成物N-(Quinoxalin-6-ylmethyl)butan-1-amineHCID 12071593—

反応条件

温度85 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06750343B2
出典データセットuspto-grants-2004_06
ORD IDord-6bd3ee9d2695469e9d5b114ef71ea79d
出典メモuspto-grants-2004_06