Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrogen Bromide → 2-Bromo-5-iodo-3-nitropyridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrogen Bromide | HCID 260 | — |
| 반응물 | Ammonium Hydroxide | HCID 14923 | — |
| 반응물 | 2-Amino-5-iodo-3-nitropyridine | HCID 3384468 | — |
| 반응물 | Sodium Nitrite | HCID 23668193 | — |
| 생성물 | 2-Bromo-5-iodo-3-nitropyridine | HCID 18619785 | 23% |
반응 단계
5-iodo-3-nitro-2-aminopyridine (5.6 g, 21.1 mmol) and concentrated HBr (60 mL) were stirred at room temperature for ten minutes. Sodium nitrite (11.7 g, 170 mmol) was then slowly added followed by CuBr (3.9 g, 27.2 mmol). Stirring continued overnight. The mixture was poured into 1:1 NH4OH:H2O, extracted with ethyl acetate, dried over sodium sulfate, then concentrated. The crude residue was purified by flash chromatography using 9:1 hexane:ethyl acetate to yield 5-iodo-3-nitro-2-bromopyridine (1.618 g, 23%) as a colorless solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07615567B2 |
| 출처 데이터셋 | uspto-grants-2009_11 |
| ORD ID | ord-68c9d6171e4c4c63aa75cb8747ad4930 |
| 출처 메모 | uspto-grants-2009_11 |