Lithium Chloride → Methyl 2-(5-bromo-3-nitropyridin-2-yl)acetate
반응식
[Br:1][C:2]1[CH:3]=[C:4]([N+:17]([O-:19])=[O:18])[C:5]([CH:8](C(OC)=O)[C:9]([O:11][CH3:12])=[O:10])=[N:6][CH:7]=1.[Cl-].[Li+]>O>[Br:1][C:2]1[CH:3]=[C:4]([N+:17]([O-:19])=[O:18])[C:5]([CH2:8][C:9]([O:11][CH3:12])=[O:10])=[N:6][CH:7]=1참가 물질
4
실험 절차
Prepared according to procedure H using dimethyl 2-(5-bromo-3-nitropyridin-2-yl)malonate (35 g, 105 mmol), lithium chloride (22.27 g, 525 mmol) and water (50 mL) and heating at reflux for 24 h. After purification methyl 2-(5-bromo-3-nitropyridin-2-yl)acetate was obtained as brown oil. Mass Spectrum (ESI) m/e=275 [(M+1) (79Br)] and 277 [(M+1) (81Br)].
후처리
- customPrepared
- temperatureheating
- temperatureat reflux for 24 h
- customAfter purification methyl 2-(5-bromo-3-nitropyridin-2-yl)acetate
- customwas obtained as brown oil
출처 및 근거
- ORD 기록
- ord-85614c93c94a4551931fdc6ba25b9cb8
- 출처 데이터셋
- uspto-grants-2014_07
- 특허 번호
- US08765940B2
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