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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 710214생성일: 2026년 10월 26일

Cesium carbonate → 3-Cyclopropyl-2-fluoro-5-nitroaniline

https://huagongshe.com/reaction/710214

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물TricyclohexylphosphineHCID 75806—
반응물2-Cyclopropyl-6-methyl-1,3,6,2-dioxazaborocane-4,8-dioneHCID 44138342—
반응물3-Bromo-2-fluoro-5-nitroanilineHCID 58065807—
촉매palladium(II) acetateHCID 167845—
용매Toluene waterHCID 22272177—
생성물3-Cyclopropyl-2-fluoro-5-nitroanilineHCID 5806580869.2%

반응 조건

온도100 °C

반응 단계

A mixture of 3-bromo-2-fluoro-5-nitroaniline (2.20 g, 9.36 mmol, 1 equiv), cyclopropylboronic acid MIDA ester (Aldrich; 11.07 g, 56.17 mmol, 6 equiv), Cy3P (1.05 g, 3.74 mmol, 0.4 equiv), Cs2CO3 (54.90 g, 168.50 mmol, 18 equiv) in toluene/H2O (5:1; 450 mL:90 mL) followed by Pd(OAc)2 (0.420 g, 1.87 mmol. 0.20 equiv) was de-gassed by sonicating under vacuum for 10 minutes and back-filled with N2. The mixture was then heated at 100° C. overnight. After allowing to cool to room temperature, the mixture was concentrated to dryness. The residue was taken in DCM, and silica gel was added at this stage so that the residue was absorbed directly on to silica gel. After removing the solvent under vacuum, the crude product was purified by column chromatography on silica gel using DCM to give the product 3-cyclopropyl-2-fluoro-5-nitroaniline (1.27 g, 69%) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09181222B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-57f0a91f5ec24e2f81ca8139a28c13a1
출처 메모uspto-grants-2015_11