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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1099056생성일: 2026년 10월 27일

6-Bromoquinoline → (Quinolin-6-yl)acetonitrile

https://huagongshe.com/reaction/1099056

반응식

참여 물질

역할이름HCID투입량
반응물6-BromoquinolineHCID 79243—
반응물(Trimethylsilyl)acetonitrileHCID 87557—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
촉매Zinc(II) fluorideHCID 10129912—
용매DimethylformamideHCID 6228—
생성물(Quinolin-6-yl)acetonitrileHCID 2199255272.1%

반응 단계

To a mixture of (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (6.7 g, 0.012 mol), tris(dibenzylideneacetone)dipalladium(0) (10.0 g, 0.012 mol), 6-bromoquinoline (120.0 g, 0.577 mol) in DMF (360 mL) in a 3-neck round bottom flask with stirring under an atmosphere of nitrogen was added (trimethylsilyl)acetonitrile (98.7 mL, 0.721 mol), followed by zinc difluoride (42 g, 0.40 mol). The flask was sealed under an atmosphere of nitrogen. The reaction was stirred at 105° C. for 20 h. After cooling the solution to RT, the reaction mixture was quenched with aqueous ammonia solution and extracted with ethyl acetate (3×500 mL). The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue was chromatographed on a silica gel column (ethyl acetate in hexanes: 0-65%) to afford the desired product quinolin-6-ylacetonitrile (70 g, 72.1%). Analytical LCMS: (M+H)+=168.9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143251B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-51ed9ee3cb0c4abb86c3caec7c5a6dad
출처 메모uspto-grants-2012_03