참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | Tricyclohexylphosphine | HCID 75806 | — |
| 반응물 | 2-Cyclopropyl-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione | HCID 44138342 | — |
| 반응물 | 3-Bromo-2-fluoro-5-nitroaniline | HCID 58065807 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Toluene water | HCID 22272177 | — |
| 생성물 | 3-Cyclopropyl-2-fluoro-5-nitroaniline | HCID 58065808 | 69.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09181222B2 |
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| 출처 데이터셋 | uspto-grants-2015_11 |
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| ORD ID | ord-57f0a91f5ec24e2f81ca8139a28c13a1 |
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| 출처 메모 | uspto-grants-2015_11 |
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