Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 178526703 | HCID 178526703 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178526832 | HCID 178526832 | 90% |
Reaction Steps
A mixture of 2-hydroxy-5-nitropyridine (50.0 g, 0.358 mol) and water (7 L) was warmed to 40° C. and bromine (21.1 mL, 0.393 mol) was added dropwise over ˜20 min. After stirring at 40° C. for 2.5 h, the mixture was cooled to 10° C. and the crude product was isolated by filtration. The solid was washed with water and dried in vacuo to give 3-bromo-2-hydroxy-5-nitropyridine as a solid (70.0 g, 90% yield). mp 212-214° C. (with decomposition); 1H NMR (CD3OD) δ 8.66 (d, J=2.9 Hz, 1H), 8.64 (d, J=2.9 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07329656B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-373b7bc8ce3b49cb87f53de28a47d0e3 |
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| Source note | uspto-grants-2008_02 |
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