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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 595737생성일: 2026년 10월 26일

Potassium Carbonate → EThyl (2E)-3-(2,6-dichloropyridin-3-yl)prop-2-enoate

https://huagongshe.com/reaction/595737

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2,6-Dichloro-3-iodopyridineHCID 2736002—
반응물(E)-Ethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)acrylateHCID 23553751—
촉매Dichloro[1,1'-bis(di-tert-butylphosphino)ferrocene]palladium(II)HCID 53384307—
용매TetrahydrofuranHCID 8028—
생성물EThyl (2E)-3-(2,6-dichloropyridin-3-yl)prop-2-enoateHCID 90341030—

반응 단계

To a solution of 2,6-dichloro-3-iodopyridine (3.0 g, 10.95 mmol), (E)-ethyl 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)acrylate (2.476 g, 10.95 mmol), and Dichloro[1,1′-bis(di-tert-butylphosphino)ferrocene]palladium (II) (0.357 g, 0.548 mmol) in THF (81 mL) was added 1M (aq) K2CO3 (54.8 mL, 54.8 mmol). A steady stream of N2 was bubbled through the resultant mixture for 5 minutes. Stirring was continued at ambient temperature for 2 h then the mixture was diluted with EtOAc and the organic layer washed successively with water (1×) and brine (1×). The organic layer was dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by silica gel column chromatography using a gradient of 0-30% EtOAc/Hexanes as eluent to give the title compound as a tan solid. 1H NMR δ (ppm) (CHCl3-d): 7.95 (1H, d, J=16 Hz), 7.90 (1H, d, J=8.1 Hz), 7.35 (1H, d, J=8.1 Hz), 6.47 (1H, d, J=16 Hz), 4.32 (2H, q, J=7.15 Hz), 1.38 (3H, t, J=7.14 Hz). MS (M+H)+: 245.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09243002B2
출처 데이터셋uspto-grants-2016_01
ORD IDord-5ecabadc1d5245c9a80235e95ca7d05e
출처 메모uspto-grants-2016_01