반응식
[CH3:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[CH:4][N:3]=1.[Se](=O)=[O:12]>O1CCOCC1>[N+:8]([C:7]1[C:2]([CH:1]=[O:12])=[N:3][CH:4]=[CH:5][CH:6]=1)([O-:10])=[O:9]참가 물질
4
실험 절차
2-Methyl-3-nitropyridine (24 g, 173.91 mmol) was dissolved in 1,4-dioxane (500 mL) and to the mixture was added selenium dioxide (23 g, 208.7 mmol) and the mixture was heated under reflux for 16 h. After completion of reaction, the mixture was cooled to rt and filtered through Celite™ and the filtrate was concentrated under reduced pressure to give thick oily mass. The oily mass was purified by silical gel column chromatography using 20% of ethyl acetate and hexane as eluent to give 3-nitro-2-pyridinecarbaldehyde as an off white solid: 1H-NMR (CDCl3) δ: 7.7 (m, 1H), 8.3 (d, 1H), 9.0 (d, 1H), 10.3 (s, 1H).
후처리
- temperaturethe mixture was heated
- temperatureunder reflux for 16 h
- customAfter completion of reaction
- filtrationfiltered through Celite™
- concentrationthe filtrate was concentrated under reduced pressure
- customto give thick oily mass
- customThe oily mass was purified by silical gel column chromatography
출처 및 근거
- ORD 기록
- ord-6125dbff90ba4f408de676406cbf1884
- 출처 데이터셋
- uspto-grants-2014_01
- 특허 번호
- US08633313B2
연결된 노트
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