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HRID 353323생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/353323

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl PeroxideHCID 7187—
반응물N-bromobutanimideHCID 67184—
반응물6-MethylquinoxalineHCID 242567—
반응물6-(Bromomethyl)quinoxalineHCID 10214510—
용매ChlorobenzeneHCID 7964—
용매PentaneHCID 8003—
용매ButylamineHCID 8007—
생성물N-(Quinoxalin-6-ylmethyl)butan-1-amineHCID 12071593—

반응 조건

온도85 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06750343B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-6bd3ee9d2695469e9d5b114ef71ea79d
출처 메모uspto-grants-2004_06