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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74158Generated: October 26, 2026

4-((Tetrahydropyran-4-yl)amino)-3-nitrobenzoic acid → 3-Amino-4-((tetrahydropyran-4-yl)amino)benzoic acid

https://huagongshe.com/reaction/74158

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-((Tetrahydropyran-4-yl)amino)-3-nitrobenzoic acidHCID 43610332—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product3-Amino-4-((tetrahydropyran-4-yl)amino)benzoic acidHCID 54888048100.2%

Reaction Steps

4-((Tetrahydropyran-4-yl)amino)-3-nitrobenzoic acid (see Working Example 4-1) (202 g, 0.76 mol) was dissolved in a solvent mixture of THF (2.2 L) and methanol (1.5 L), Pd/C (5%, wet, 20 g) was added, and hydrogenation was carried out under 5 atm. Hydrogen absorption stopped at 3 h, and after the system was purged with argon the catalyst was removed by filtration, and the filtrate was concentrated at reduced pressure to yield the title compound (180 g, quant.) as a dark gray solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829035B2
Source datasetuspto-grants-2014_09
ORD IDord-b340ee561d764d2ea478af19f7930b3d
Source noteuspto-grants-2014_09