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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4039생성일: 2026년 10월 25일

Sodium Hydroxide → 6-Bromo-(2-nitrophenyl)-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/4039

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물N-bromobutanimideHCID 67184—
반응물1-(2-Nitrophenyl)-1,2,3,4-tetrahydroquinolineHCID 13812926—
용매DimethylformamideHCID 6228—
생성물6-Bromo-(2-nitrophenyl)-1,2,3,4-tetrahydroquinolineHCID 1381292882.7%

반응 단계

A stirred solution, under nitrogen, of 1-(2-nitrophenyl)-1,2,3,4-tetrahydroquinoline (76.3 g, 0.30 mole) in dimethylformamide (1000 ml) was cooled to -10° C. A solution of of N-bromosuccinimide (58.7 g, 0.33 mole) in dimethylformamide (250 ml) was added dropwise at such a rate as to keep the reaction temperature below 0° C. (1.5 hours). Half-an hour after the addition was completed, the reaction mixture was poured into 7 liters of 2N-sodium hydroxide solution/ice, with stirring. The product separated as an oil. The quench fluids were decanted and the oil was rinsed several times with water. The oil was dissolved in dichloromethane (1.5 l). The organic solution was extracted once with 2N-sodium hydroxide solution, thrice with water, dried over sodium sulfate and concentrated. The residue was dissolved in 1:1 hexane:toluene (250 ml) and the solution was absorbed on a chromatography column containing 2 kg of silica gel packed in 1:1 hexane:toluene. Elution with this solvent mixture provided 82.7 g (82%) of product, as an oil. For analysis, a sample was Kugelrohr distilled at a vessel temperature of 166°-168° C. (0.2 mm Hg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04723007
출처 데이터셋uspto-grants-1988_02
ORD IDord-c2f682b48eea413db9b847972f11227f
출처 메모uspto-grants-1988_02