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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17931생성일: 2026년 10월 26일

Benzoyl Peroxide → 6-(Bromomethyl)quinoxaline

https://huagongshe.com/reaction/17931

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl PeroxideHCID 7187—
반응물N-bromobutanimideHCID 67184—
반응물6-MethylquinoxalineHCID 242567—
용매Carbon TetrachlorideHCID 5943—
생성물6-(Bromomethyl)quinoxalineHCID 1021451077.5%

반응 단계

To a solution of 6-methylquinoxaline (10.0 g, 69.4 mmol) in CCl4 (80 mL) was added NBS (13.5 g, 76.3 mmol) and benzoyl peroxide (BP, 1.7 g, 6.9 mmol) at room temperature. The mixture was heated at reflux for 2 hours. After cooling, the mixture was evaporated under vacuum to give a yellow solid, which was extracted with Petroleum Ether (50 mL×5). The extracts were concentrated under vacuum. The organics were combined and concentrated to give crude 6-bromomethylquinoxaline (12.0 g), which was used directly in the next step. 1H NMR (300 MHz, CDCl3) δ 8.85-8.87 (m, 2H), 8.10-8.13 (m, 2H), 7.82 (dd, J=2.1, 8.7 Hz, 1H), 4.70 (s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741321B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-dbdee4d6eed2475087add1eab84006da
출처 메모uspto-grants-2010_06