Diethyl Malonate → 3-Bromo-2-methyl-5-nitropyridine
반응식
[C:1](OCC)(=O)CC(OCC)=O.[H-].[Na+].[Br:14][C:15]1[C:16](Cl)=[N:17][CH:18]=[C:19]([N+:21]([O-:23])=[O:22])[CH:20]=1.OC1C=CC([N+]([O-])=O)=CN=1>C(OCC)C>[Br:14][C:15]1[C:16]([CH3:1])=[N:17][CH:18]=[C:19]([N+:21]([O-:23])=[O:22])[CH:20]=1참가 물질
반응 조건
- 온도
- 100 °C
실험 절차
A solution of diethyl malonate (17.6 mL, 0.116 mol) in diethyl ether (250 mL) at ambient temperature was treated with sodium hydride (80% in mineral oil, 3.5 g, 0.116 mol), and the mixture was stirred for 1 hour. Then 3-bromo-2-chloro-5-nitropyridine (25 g, 105 mmol; prepared from 2-hydroxy-5-nitropyridine according to the procedure of V. Koch and S. Schnatterer, Synthesis 1990, 499-501) was added in portions over 5 minutes. After the mixture had stirred for 1 hour, the solvent was evaporated, and the residue was heated at 100° C. for 1 hour. After the mixture had cooled, 12 N H2SO4 was added, and the mixture was heated at reflux for about 16 hours. The mixture was allowed to cool to ambient temperature, then further cooled as it was treated with 50% NaOH to give an alkaline pH. The resulting solution was extracted with CHCl3 (3×), and the organic extracts were washed with H2O, dried (MgSO4) and evaporated to afford 17.1 g of the title compound as a red oil: 1H NMR (CDCl3, 300 MHz) δ 2.81 (s, 3H), 8.61 (d, J=2 Hz, 1H), 9.26 (d, J=2 Hz, 1H).
후처리
- customSchnatterer, Synthesis 1990, 499-501)
- additionwas added in portions over 5 minutes
- stirringAfter the mixture had stirred for 1 hour
- customthe solvent was evaporated
- temperatureAfter the mixture had cooled
- addition12 N H2SO4 was added
- temperaturethe mixture was heated
- temperatureat reflux for about 16 hours
- temperatureto cool to ambient temperature
- temperaturefurther cooled as it
- additionwas treated with 50% NaOH
- customto give an alkaline pH
- extractionThe resulting solution was extracted with CHCl3 (3×)
- washthe organic extracts were washed with H2O
- dry with materialdried (MgSO4)
- customevaporated
출처 및 근거
- ORD 기록
- ord-0e7e1e73a9a24df5bc11a9ec9e1880f9
- 출처 데이터셋
- uspto-grants-2000_10
- 특허 번호
- US06133253
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