HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 2-Bromo-5-iodo-3-nitropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 2-Amino-5-iodo-3-nitropyridine | HCID 3384468 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Product | 2-Bromo-5-iodo-3-nitropyridine | HCID 18619785 | 23% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07615567B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-68c9d6171e4c4c63aa75cb8747ad4930 |
| Source note | uspto-grants-2009_11 |