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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1019821생성일: 2026년 10월 24일

Phosphorus oxychloride → 2-(1-Bromoethyl)-3-chloro-6-fluoroquinoxaline

https://huagongshe.com/ko/reaction/1019821

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참여 물질

역할이름HCID투입량
반응물Phosphorus oxychlorideHCID 24813—
반응물3-(1-bromoethyl)-7-fluoroquinoxalin-2(1H)-oneHCID 86698519—
생성물2-(1-Bromoethyl)-3-chloro-6-fluoroquinoxalineHCID 8669852092.8%

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온도100 °C

반응 단계

A heterogeneous mixture of 3-(1-bromoethyl)-7-fluoroquinoxalin-2(1H)-one (58.86 g, 217.1 mmol) and phosphorous oxychloride (198.8 ml, 2171 mmol) in a 1 L round bottom flask was stirred at 100° C. for 2 h. The mixture was heterogeneous in the beginning of the reaction and then homogeneous black solution over 1 h. After 2 h, the mixture was cooled to rt and concentrated under reduced pressure. To the black residue was carefully added ice (˜400 ml) in portions and then water (200 ml) with stirring. The mixture was neutralized with NH4OH (200 ml) and ice (˜200 ml) with stirring. The resulting precipitate was collected by filtration, rinsed with water (1 L), and dried under high vacuum overnight to give 2-(1-bromoethyl)-3-chloro-6-fluoroquinoxaline (58.31 g, 92.8% yield) including 3-chloro-2-(1-chloroethyl)-6-fluoroquinoxaline as a brown solid. 1H NMR (400 MHz, DMSO-d6), ratio of bromoethyl analog and chloroethyl analog=2.5:1 Mass Spectrum (ESI) m/e=288.9 [M+H(79Br)]+ and 291.0 [M+H (81Br)]+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08716290B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-86e02f9c3a284b659a42addacb36b686
출처 메모uspto-grants-2014_05