돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29082생성일: 2026년 10월 24일

2,6-Dibromopyridine → n-[1-Eth-(z)-ylidene-5,5-dimethoxy-2-oxo-pentyl]acrylimidoyl bromide

https://huagongshe.com/ko/reaction/29082

반응식

참여 물질

역할이름HCID투입량
반응물2,6-DibromopyridineHCID 12274—
반응물4,4,N-Trimethoxy-N-methylbutyramideHCID 59788083—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
생성물n-[1-Eth-(z)-ylidene-5,5-dimethoxy-2-oxo-pentyl]acrylimidoyl bromideHCID 8723332374.9%

반응 조건

온도-70 °C

반응 단계

To a suspension of 2,6-dibromopyridine(8.1 g, 34.03 mmol) in 80 mL of ether at −70° C., is added BuLi(12.3 mL, 26.17 mmol, 2.5 M in Hexane) in on portion. After stirring at −70° C. for 5 min, 4,4,N-Trimethoxy-N-methyl-butyramide(5.0 g, 26.17 mmol) is added to the solution dropwise. After stirring at −70° C. for 1.5 hr, the reaction mixture is quenched with 120 mL of water and extracted with 3×130 mL of EtOAc. The combined organic layers is concentrated and purified by chromatography(Hexane/EtOAc:70/30) to give N-[1-Eth-(Z)-ylidene-5,5-dimethoxy-2-oxo-pentyl]-acrylimidoyl bromide(5.96 g, 60.5%) as light yellow liquid. M/Z=288.0

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419975B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-4fd606995a9a445d89b0c7983409a85d
출처 메모uspto-grants-2008_09