HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Nitro-2-phenoxypyridine → N-Hydroxy-2-phenoxypyridin-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Nitro-2-phenoxypyridine | HCID 901896 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | 4-Methylmorpholine | HCID 7972 | — |
| Product | N-Hydroxy-2-phenoxypyridin-3-amine | HCID 21831171 | — |
Reaction Steps
A mixture of 9.2 g (43 mmol) of 3-nitro-2-phenoxypyridine (Example 1.a) and 100 ml of N-methylmorpholine was hydrogenated at room temperature (approximately 25° C.) and an H2 pressure of approximately 1.1 bar in the presence of 1 g of 5% platinum/charcoal (51% water; manufactured by Degussa). The hydrogen uptake ceased after approximately 2 hours. The catalyst was removed by filtration through active charcoal. The resulting solution was freed from solvent under reduced pressure ("high vacuum"). This gave 7.8 g (90%) of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05977146 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-e70011adb901483ea4f138c98a1436b1 |
| Source note | uspto-grants-1999_11 |