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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259932Generated: October 31, 2026

4,6-Dichloro-3-hydroxy-2-nitrobenzoic acid → HCID 86749538, compound

https://huagongshe.com/reaction/259932

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6-Dichloro-3-hydroxy-2-nitrobenzoic acidHCID 10658432—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 86749538HCID 8674953828.1%

Reaction Steps

4,6-Dichloro-3-hydroxy-2-nitrobenzoic acid (223 mg, 0.88 mmol) was dissolved in EtOH (50 mL) and Pd/C (10%, 30 mg) was added. Hydrogenation at atmospheric pressure and at room temperature for 1 h, filtration and evaporation of the solvent gave 205 mg of crude product. Purification by column chromatography (SiO2, EtOAc-HOAc 50:1) gave a residue which was recrystallized from MeOH/water (0.5/1.5 mL). Column chromatography (SiO2, EtOAc-HOAc 400:1) followed by dissolving the free amine in THF (0.6 mL) and precipitating the hydrochloride by adding HCl/Et2O (3M, 1 mL) and Et2O (1 mL) gave 4,6-dichloro-3-hydroxyanthranilic acid hydrochloride (32 mg). Mp: 231° C. (dec.). 1H NMR (DMSO-d6): δ7.0 (br, 5H), 6.68 (s, 1H). 13C NMR (DMSO-d6): δ167.15, 140.27, 139.05, 122.49, 121.88, 116.24, 113.99. MS (EI, 70 eV): m/z (rel. int.) 223/221 (M+, 42/65).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05523475
Source datasetuspto-grants-1996_06
ORD IDord-dd574f7b285742ac81acf1c0392d8587
Source noteuspto-grants-1996_06