Ethanol → HCID 86628514, 화합물
반응식
[Cl-].[NH4+].[Br:3][C:4]1[CH:5]=[C:6]([O:13][CH3:14])[C:7]([N+:10]([O-])=O)=[N:8][CH:9]=1.[CH2:15]([OH:17])C>O.[Fe]>[Br:3][C:4]1[CH:5]=[C:6]([O:13][CH3:14])[C:7]([NH:10][CH:15]=[O:17])=[N:8][CH:9]=1참가 물질
반응 조건
- 온도
- 85 °C
실험 절차
Iron (67.3 g) and ammonium chloride (129 g) were added to a solution of 5-bromo-3-methoxy-2-nitropyridine (56.0 g, CAS #152684-26-9) in ethanol (500 mL) and water (200 mL). The reaction solution was stirred at 80 to 90° C. for one hour and then left to cool to room temperature. The reaction solution was filtered through celite and washed with ethanol. Then, the filtrate was concentrated under reduced pressure. The residue was diluted with ethyl acetate and water, and the organic layer was separated. The resulting organic layer was washed with brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was diluted with THF (84 mL). The THF solution was added dropwise to a mixed solution of formic acid (78.1 mL) and acetic anhydride (78.3 mL) at room temperature. Then, the reaction solution was stirred for one hour. Ice water (500 mL) was added to the reaction solution, and the precipitated crystals were collected by filtration. The crystals were washed with water and then air-dried. The crystals were recrystallized from toluene to obtain 34.1 g of the title compound. The property values of the compound are as follows.
후처리
- waitleft
- temperatureto cool to room temperature
- filtrationThe reaction solution was filtered through celite
- washwashed with ethanol
- concentrationThen, the filtrate was concentrated under reduced pressure
- additionThe residue was diluted with ethyl acetate and water
- customthe organic layer was separated
- washThe resulting organic layer was washed with brine
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
- additionThe residue was diluted with THF (84 mL)
- additionThe THF solution was added dropwise to a mixed solution of formic acid (78.1 mL) and acetic anhydride (78.3 mL) at room temperature
- stirringThen, the reaction solution was stirred for one hour
- additionIce water (500 mL) was added to the reaction solution
- filtrationthe precipitated crystals were collected by filtration
- washThe crystals were washed with water
- customair-dried
- customThe crystals were recrystallized from toluene
출처 및 근거
- ORD 기록
- ord-43bc8a557ab743afbf13ad67e5120c0f
- 출처 데이터셋
- uspto-grants-2014_06
- 특허 번호
- US08754100B2
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