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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63253생성일: 2026년 10월 24일

Ethyl bromodifluoroacetate → Ethyl 2-(5-(4-cyanophenoxy)pyridin-2-yl)-2,2-difluoroacetate

https://huagongshe.com/ko/reaction/63253

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromodifluoroacetateHCID 69585—
반응물4-((6-Bromopyridin-3-yl)oxy)benzonitrileHCID 45142267—
촉매CopperHCID 23978—
용매Dimethyl SulfoxideHCID 679—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 2-(5-(4-cyanophenoxy)pyridin-2-yl)-2,2-difluoroacetateHCID 9005222356.5%

반응 단계

A mixture of ethyl 2-bromo-2,2-difluoroacetate (22.13 mL, 109.05 mmol) and copper (13.85 g, 218.1 mmol) in dry dimethylsulfoxide (DMSO) (80 mL) was stirred at room temperature (rt) for 4 h. 4-((6-Bromopyridin-3-yl)oxy)benzonitrile (10 g, 36.35 mmol) was added and the mixture heated at 50° C. for 16 h. The reaction mixture was cooled to room temperature, diluted with 200 mL of ethyl acetate (EtOAc) and stirred for 10 min. The mixture was filtered through a plug of Celite® and the filtrate was washed with saturated NH4Cl solution to remove any remaining copper. The solution was dried (Na2SO4) and solvent was removed under reduced pressure to give the title compound as brown oil (6.5 g, 56.5%): IR (thin film) 2229, 1767 cm−1; 1H NMR (300 MHz, CDCl3) δ 8.44 (d, J=2.7 Hz, 1H), 7.78 (d, J=8.7 Hz, 1H), 7.73-7.64 (m, 2H), 7.49 (dd, J=8.6, 2.7 Hz, 1H), 7.16-7.07 (m, 2H), 4.39 (q, J=7.1 Hz, 2H), 1.35 (t, J=7.2 Hz, 3H); ESIMS m/z 319 ([M+H]+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447073B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-02423e094bc241c49175ffd10b6637c0
출처 메모uspto-grants-2016_09