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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 71909생성일: 2026년 10월 24일

Water → Pyrrolidine-1,2-dicarboxylic acid 2-{2-[7-(2-bromo-acetyl)-dibenzofuran-3-yl]-2-oxo-ethyl}ester 1-tert-butyl ester

https://huagongshe.com/ko/reaction/71909

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물N-bromobutanimideHCID 67184—
반응물(Z)-1-Ethoxy-2-(tributylstannyl)etheneHCID 2763294—
반응물Pyrrolidine-1,2-dicarboxylic acid 2-[2-(7-bromo-dibenzofuran-3-yl)-2-oxo-ethyl] ester 1-tert-butyl esterHCID 66621169—
촉매HCID 178418476HCID 178418476—
용매1,4-DioxaneHCID 31275—
생성물Pyrrolidine-1,2-dicarboxylic acid 2-{2-[7-(2-bromo-acetyl)-dibenzofuran-3-yl]-2-oxo-ethyl}ester 1-tert-butyl esterHCID 7233831875.3%

반응 조건

온도80 °C

반응 단계

To the solution of Pyrrolidine-1,2-dicarboxylic acid 2-[2-(7-bromo-dibenzofuran-3-yl)-2-oxo-ethyl]ester 1-tert-butyl ester (250 mg, 0.5 mmol) and tributyl(ethoxyvinyl)stannane (188 μl, 0.55 mmol) in dioxane (3.3 ml) was added PdCl2(PPh3)2 (15 mg). The mixture was heated at 80° C. for 16 hours and was cooled to 0° C. Water (1.1 ml) was added, followed by slow addition of NBS (98 mg, 0.55 mmol) over 5 minutes period. The mixture was stirred at 0° C. for additional 40 minutes, and the solvent was removed under reduced pressure. The mixture was diluted with EtOAc, and was washed with water and brine and dried with sodium sulfate. Concentration and purification by flash column chromatography (hexane/EtOAc) gave Pyrrolidine-1,2-dicarboxylic acid 2-{2-[7-(2-bromo-acetyl)-dibenzofuran-3-yl]-2-oxo-ethyl}ester 1-tert-butyl ester (205 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822430B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-b17f54ef654d4bdf800a9b3ff3e44d59
출처 메모uspto-grants-2014_09