돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4043생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/4043

반응식

참여 물질

역할이름HCID투입량
반응물2,4,6-TrimethylpyridineHCID 7953—
반응물1,2,3,4-TetrahydroquinolineHCID 69460—
반응물1,4-Dibromo-2-nitrobenzeneHCID 77004—
용매1,2,3-TrimethylbenzeneHCID 10686—
생성물1-(4-Bromo-2-nitrophenyl)-1,2,3,4-tetrahydroquinolineHCID 1381292718%

반응 단계

A stirred mixture, under nitrogen, of 2,5-dibromonitrobenzene (140.5 g, 0.50 mole), 1,2,3,4-tetrahydroquinoline (133.2 g, 1.00 mole) and symmetrical collidine (121.2 g, 1.00 mole) in 1,2,3-trimethylbenzene (500 ml) as solvent was heated at 160°-165° C. for 7 days. The mixture was cooled to room temperature, filtered, and the filtrate was concentrated in vacuo (100° C.). The residue was taken up in dichloromethane (1.5 l) and the solution was extracted three times with dilute hydrochloric acid, once with dilute sodium hydroxide solution, three times with water, dried over anhydrous sodium sulfate and concentrated. This residue was dissolved in 1:1 hexane:toluene (250 ml) and adsorbed on a chromatography column containing 3 kg of silica gel. Elution with 1:1 hexane:toluene gave 30 g (18%) of product, as an oil. A portion of the oil was Kugelrohr distilled at an oven-temperature of 163°-165° C. (0.1 mm Hg) to provide the analytical sample.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04723007
출처 데이터셋uspto-grants-1988_02
ORD IDord-16910464cc86414581b08344acd38357
출처 메모uspto-grants-1988_02