HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitropyridin-2-ylamine → 2-Bromo-3-nitropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitropyridin-2-ylamine | HCID 77887 | — |
| Reactant | 2,3-Dibromopyridine | HCID 817102 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Product | 2-Bromo-3-nitropyridine | HCID 555054 | — |
Reaction Steps
Bouillon et al in Tetrahedron, 2002, 58, 17, 3323-3328 reported a three-step process for the preparation of 2,3-dibromopyridine from 2-amino-3-nitropyridine. The process involves diazotization of 2-amino-3-nitropyridine followed by addition of CuBr in 47% HBr to obtain 2-bromo-3-nitropyridine. The 2-bromo-3-nitropyridine so obtained is reduced with Fe and acetic acid to 3-amino-2-bromopyridine and subsequent diazotization to give 2,3-dibromopyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08293918B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-7b0313d5e5e14bca9d9eb20cacab75c0 |
| Source note | uspto-grants-2012_10 |