반응식
[Br:1][C:2]1[CH:7]=[C:6](N)[C:5]([N+:9]([O-:11])=[O:10])=[C:4]([Br:12])[N:3]=1.N([O-])=O.[Na+].[ClH:17]>>[Br:1][C:2]1[CH:7]=[C:6]([Cl:17])[C:5]([N+:9]([O-:11])=[O:10])=[C:4]([Br:12])[N:3]=1참가 물질
4
반응 조건
- 온도
- 0 °C
실험 절차
2,6-Dibromo-4-amino-5-nitro-pyridine (3 g) was taken up in concentrated hydrochloric acid (20 mL) and cooled to 0° C. Sodium nitrite (3.5 g) was added and the reaction mixture was allowed to stir at 0° C. for 1 h. The ice bath was removed and the reaction allowed to warm to room temperature over 3 h, and was then quenched by the addition of ethyl acetate (50 mL) and water (100 mL). The organic layer was separated, dried over MgSO4 and filtered and evaporated in vacuo to a pale yellow oil, which was purified by column chromatography using 35:1 pentane:EtOAc as eluant to give the title compound (2.2 g) as a white solid.
후처리
- customThe ice bath was removed
- temperatureto warm to room temperature over 3 h
- customwas then quenched by the addition of ethyl acetate (50 mL) and water (100 mL)
- customThe organic layer was separated
- dry with materialdried over MgSO4
- filtrationfiltered
- customevaporated in vacuo to a pale yellow oil, which
- customwas purified by column chromatography
출처 및 근거
- ORD 기록
- ord-8f145f331fea473dbe193015c2f9acc9
- 출처 데이터셋
- uspto-grants-2010_04
- 특허 번호
- US07691877B2
연결된 노트
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