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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55749Generated: October 24, 2026

3-Nitrophthalic acid → 3-Aminophthalic acid

https://huagongshe.com/en/reaction/55749

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitrophthalic acidHCID 69043—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-Aminophthalic acidHCID 7949084%

Reaction Steps

10% Pd/C (2.5 g), 3-nitrophthalic acid (75.0 g, 355 mmol) and ethanol (1.5 L) were charged to a 2.5 L Parr hydrogenator under a nitrogen atmosphere. Hydrogen was charged to the reaction vessel for up to 55 psi. The mixture was shaken for 13 hours, maintaining hydrogen pressure between 50 and 55 psi. Hydrogen was released and the mixture was purged with nitrogen 3 times. The suspension was filtered through a celite bed and rinsed with methanol. The filtrate was concentrated in vacuo. The resulting solid was reslurried in ether and isolated by vacuum filtration. The solid was dried in vacuo to a constant weight, affording 54 g (84% yield) of 3-aminophthalic acid as a yellow product. 1H-NMR (DMSO-d6) δ: 3.17 (s, 2H), 6.67 (d, 1H), 6.82 (d, 1H), 7.17 (t, 1H), 8-10 (br, s, 2H); 13C-NMR (DMSO-d6) δ: 112.00, 115.32, 118.20, 131.28, 135.86, 148.82, 169.15, 170.09.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09433606B2
Source datasetuspto-grants-2016_09
ORD IDord-aac163278d774f779aaceb5fc6c049d3
Source noteuspto-grants-2016_09