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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5681생성일: 2026년 10월 23일

2-Bromobenzonitrile → 4-[(2'-Cyanobiphenyl-4-yl)methoxy]-2-ethyl-5,6,7,8-tetrahydroquinoline

https://huagongshe.com/ko/reaction/5681

반응식

참여 물질

역할이름HCID투입량
반응물2-BromobenzonitrileHCID 16272—
반응물4-[(2-Ethyl-5,6,7,8-tetrahydroquinolin-4-yl)oxymethyl]phenylboronic acidHCID 15171422—
촉매HCID 178418397HCID 178418397—
용매TolueneHCID 1140—
용매Sodium CarbonateHCID 10340—
생성물4-[(2'-Cyanobiphenyl-4-yl)methoxy]-2-ethyl-5,6,7,8-tetrahydroquinolineHCID 1979640849.4%

반응 단계

Tetrakis(triphenylphosphine)palladium (40 mg) was added to a suspension of 4-[(2-ethyl-5,6,7,8-tetrahydroquinolin-4-yl)oxymethyl]-phenylboronic acid (200 mg) and 2-bromobenzonitrile (106 mg) in toluene (2 ml) ethanol (0.5 ml) and 2M aqueous sodium carbonate (0.58 ml). The mixture was degassed and placed under an atmosphere of argon, then heated under reflux for 12 hours. The resulting solution was cooled to ambient temperature, and dichloromethane (30 ml) and water (10 ml) were added. The organic layer was separated, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by flash chromatography, eluting with ethyl acetate/hexane (3:1 v/v), and the product triturated with ether/hexane to give 4-[(2'-cyanobiphenyl-4-yl)methoxy]-2-ethyl-5,6,7,8-tetrahydroquinoline (106 mg) as a white solid, m.p. 147°-148° C.; NMR (CDCl3): 1.29(t,3H), 1.7-1.95(m,4H), 5.17(s,2H), 6.57(s,1H), 7.4-7.7 (complex m,7 H), 7.78(d,1H); mass spectrum (+ve CI) 369 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245035
출처 데이터셋uspto-grants-1993_09
ORD IDord-f2e47c7899134a9295da63016e60ddb0
출처 메모uspto-grants-1993_09