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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29689Generated: October 29, 2026

Ammonium formate → Methyl 2-amino-4-hydroxybenzoate

https://huagongshe.com/reaction/29689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantMethyl 4-hydroxy-2-nitrobenzoateHCID 21082409—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductMethyl 2-amino-4-hydroxybenzoateHCID 2032795696.1%

Reaction Steps

To a stirred solution of 4-hydroxy-2-nitrobenzoic acid methyl ester (4.410 g, 22.369 mmol) in methanol (80 ml) under nitrogen at room temperature was added ammonium formate (5.642 g, 89.475 mmol) and 5% Pd/C (450 mg). After 5 hours the reaction mixture was filtered through celite and rinsed. The filtrate was concentrated and the residue partitioned between EtOAc (150 ml) and water (40 ml). The layers were shaken, separated and the organic layer washed with water (3×30 ml), brine (2×30 ml), dried over Na2SO4, filtered, concentrated and dried to give 2-amino-4-hydroxy-benzoic acid methyl ester (3.593 g, 21.494 mmol, 96%) as an off-white solid, dec. 113-118° C. 1H NMR (DMSO-d6) δ 3.70 (s, 3H), 5.98 (dd, 1H), 6.10 (s, 1H), 6.59 (s, 1H), 7.54 (d, 1H), 9.81 (s, 1H); mass spectrum [ES(−)], m/z 166 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420083B2
Source datasetuspto-grants-2008_09
ORD IDord-91d40f49a0f447af955b74f8cc603733
Source noteuspto-grants-2008_09