HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Dioxide → 2-Amino-5-bromo-3-hydroxypyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-Bromo-3H-oxazolo(4,5-b)pyridin-2-one | HCID 13614458 | — |
| Product | 2-Amino-5-bromo-3-hydroxypyridine | HCID 11694041 | 98% |
Reaction Steps
6-Bromo-3H-oxazolo[4,5-b]pyridin-2-one (21.5 g, 100 mmol) was suspended in NaOH solution (2N, 250 mL, 500 mmol). The mixture was refluxed overnight and a clear solution was obtained. After cooling to room temperature, the reaction solution was neutralized to pH ˜7. A lot of CO2 was released and also precipitate was observed. The product was filtered, washed with water, and dried under high vacuum to provide 2-amino-5-bromo-pyridin-3-ol as an off-white solid (17.8 g, 98% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106197B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-20957d17eeb84283aadbac6a352ddb3c |
| Source note | uspto-grants-2012_01 |