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HRID 500146생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/500146

반응식

참여 물질

역할이름HCID투입량
반응물6-BromoquinolineHCID 79243—
반응물(Trimethylsilyl)acetonitrileHCID 87557—
반응물1,1'-(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 21992552—

반응 단계

To a mixture of (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (6.7 g, 12 mmol), tris(dibenzylideneacetone)dipalladium(0) (10 g, 12 mmol), 6-bromoquinoline (120 g, 577 mmol) in N,N-dimethylformamide (360 mL) in a 3-neck round bottom flask with stirring under positive nitrogen pressure was added (trimethylsilyl)acetonitrile (98.7 mL, 721 mmol), followed by zinc difluoride (42 g, 400 mmol). The flask was sealed under an atmosphere of nitrogen. The reaction mixture was stirred at 105° C. for 20 h. After cooling the solution to RT, the reaction mixture was quenched with an aqueous ammonia solution and extracted with ethyl acetate (3×500 mL). The combined organic extracts were washed with brine, dried over sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified under flash chromatography eluting with ethyl acetate in hexanes (0-65%) to afford the desired product. (70 g, 72.1%) LCMS: (M+H)=168.9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07767675B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-b522493b9eaf49899493fe9ea68b0b38
출처 메모uspto-grants-2010_08