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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75383생성일: 2026년 10월 25일

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 3-ethyl-7-fluoroquinoxalin-2(1H)-one

https://huagongshe.com/reaction/75383

반응식

참여 물질

역할이름HCID투입량
반응물2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
반응물1,4-DioxaneHCID 31275—
반응물3-ethyl-7-fluoro-3,4-dihydroquinoxalin-2(1H)-oneHCID 77623601—
용매WaterHCID 962—
용매Sodium BicarbonateHCID 516892—
생성물3-ethyl-7-fluoroquinoxalin-2(1H)-oneHCID 6728920594.8%

반응 단계

To a homogeneous solution of 3-ethyl-7-fluoro-3,4-dihydroquinoxalin-2(1H)-one (60.61 g, 312.1 mmol) and 1,4-dioxane (1350 ml) was added 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (75.91 g, 327.7 mmol) and the mixture was stirred using an overhead stirrer at rt for 2.5 h. At this time, the mixture was concentrated under reduced pressure to give a brown residue. The brown residue was suspended in saturated aqueous NaHCO3 (2 L), stirred for 30 min, filtered, washed with saturated aqueous NaHCO3 (1 L) to give a light green solid. The light green solid was re-suspended in saturated aqueous NaHCO3 (500 mL), well mixed, filtered, and washed with saturated aqueous NaHCO3 (500 mL) to give an off-white solid. The off-white solid was suspended in water (500 mL), well mixed, filtered, washed with water (1 L), air-dried overnight, and dried under high vacuum at 22° C. for 2 h to give 3-ethyl-7-fluoroquinoxalin-2(1H)-one (56.87 g, 94.8% yield) as an off-white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 12.36 (br. S, 1H), 7.76 (dd, J=9.0, 5.9 Hz, 1H), 7.11 (td, J=8.8, 2.7 Hz, 1H), 7.00 (dd, J=9.6, 2.7 Hz, 1H), 2.78 (q, J=7.4 Hz, 2H), 1.20 (t, J=7.4 Hz, 3H) Mass Spectrum (ESI) m/e=193.0 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835432B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-51e43186795f4c46b32665ec70c1ad62
출처 메모uspto-grants-2014_09