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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 417594생성일: 2026년 10월 25일

N-bromobutanimide → HCID 66620898, 화합물

https://huagongshe.com/reaction/417594

반응식

참여 물질

역할이름HCID투입량
반응물N-bromobutanimideHCID 67184—
반응물DiisopropylethylamineHCID 81531—
반응물1-[(Tert-butoxy)carbonyl]pyrrolidine-2-carboxylic acidHCID 268472—
반응물Stannane, tributyl(1-ethoxyethenyl)-HCID 619414—
반응물2,7-Dibromo-9,10-dihydrophenanthreneHCID 2825053—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물HCID 66620898HCID 66620898—

반응 조건

온도80 °C

반응 단계

Pd(Ph3)4 (347 mg, 0.3 mmol) and PdCl2(Ph3)2 (210 mg, 0.3 mmol) were added to a mixture 2,7-dibromo-9,10-dihydro-phenanthrene (2.5 g, 7.4 mmol) and tributyl(1-ethoxyvinyl)tin (2.5 mL, 7.4 mL) in 70 mL dioxane. The reaction mixture was flushed with nitrogen, heated at 80° C. for 16 hours, then cooled to ambient temperature. Water (20 mL) and NBS (1.39 g, 7.8 mmol) were added and the mixture was stirred at room temperature for 40 minutes, then diluted with ethyl acetate (300 mL). Washed with water and brine, dried over Na2SO4, filtered and concentrated in vacuo. The obtained residue was suspended in acetonitrile (70 mL). To it was added a solution of pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester (3.2 g, 14.9 mmol) and DIPEA (2.4 mL, 14.1 mmol) in 20 mL acetonitrile. The mixture was stirred at room temperature for 16 hours, then diluted with ethyl acetate (300 mL). The organic layer was washed with NaHCO3 solution and water, dried over Na2SO4, filtered and concentrated in vacuo. The obtained residue was purified by flash chromatography to provide the desired product pyrrolidine-1,2-dicarboxylic acid 2-[2-(7-bromo-9,10-dihydro-phenanthren-2-yl)-2-oxo-ethyl]ester 1-tert-butyl ester as a white solid (1.76 g, 46% over two steps). m/z 514.2, 516.2 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08088368B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-d3c2da3fe2584829963776cf7cbb18d7
출처 메모uspto-grants-2012_01