Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050727Generated: November 3, 2026

Ethanol → 3-Aminophthalic acid

https://huagongshe.com/reaction/1050727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant3-Nitrophthalic acidHCID 69043—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventDiethyl EtherHCID 3283—
Product3-Aminophthalic acidHCID 7949084%

Reaction Steps

After a mixture of 10% Pd/C (2.5 g), 3-nitrophthalic acid (75.0 g, 355 mmol) and ethanol (1.5 L) was charged to a 2.5 L Parr hydrogenator under nitrogen, hydrogen was charged to the reaction vessel for up to 55 psi (379 kPa). The mixture was shaken for 13 hours while the hydrogen pressure was maintained at between 50 psi (245 kPa) and 55 psi (379 kPa). 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 vacuum to yield a solid. The solid was suspended in ether and isolated by vacuum filtration. The solid was dried in vacuum to a constant weight to afford 54 g (84% yield) of 3-aminopthalic acid as a yellow product. The product in DMSO-d6 was characterized by a 1H NMR spectrum showing the following chemical shifts (δ in ppm): 3.17 (s, 2H), 6.67 (d, 1H), 6.82 (d, 1H), 7.17 (t, 1H), 8-10 (brs, 2H). The product in DMSO-d6 was characterized by a 13C-NMR spectrum showing the following chemical shifts (δ in ppm): 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 numberUS09387195B2
Source datasetuspto-grants-2016_07
ORD IDord-11ffbe7bf0914a7fb9460c21e79ed8e8
Source noteuspto-grants-2016_07