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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32779Generated: October 26, 2026

3-Nitrophthalic acid → 3-Aminophthalic acid

https://huagongshe.com/reaction/32779

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 vacua to a constant weight, affording 54 g (84% yield) of 3-aminopthalic 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 (brs, 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 numberUS07427638B2
Source datasetuspto-grants-2008_09
ORD IDord-6d65cc5485e74a759a1e487207bb97d3
Source noteuspto-grants-2008_09