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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601139Generated: November 2, 2026

3-Nitro-2-phenoxypyridine → N-Hydroxy-2-phenoxypyridin-3-amine

https://huagongshe.com/reaction/1601139

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitro-2-phenoxypyridineHCID 901896—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
Solvent4-MethylmorpholineHCID 7972—
ProductN-Hydroxy-2-phenoxypyridin-3-amineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977146
Source datasetuspto-grants-1999_11
ORD IDord-e70011adb901483ea4f138c98a1436b1
Source noteuspto-grants-1999_11