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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1821757Generated: November 2, 2026

4-Nitro-3-(pyridin-3-ylmethoxy)-benzoic acid methyl ester → 4-Amino-3-(pyridin-3-ylmethoxy)-benzoic acid methyl ester

https://huagongshe.com/reaction/1821757

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitro-3-(pyridin-3-ylmethoxy)-benzoic acid methyl esterHCID 67256051—
CatalystZincHCID 23994—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
SolventAmmonium ChlorideHCID 25517—
Product4-Amino-3-(pyridin-3-ylmethoxy)-benzoic acid methyl esterHCID 4338018897%

Reaction Steps

To a stirred, cooled (about 0° C.) solution of 4-nitro-3-(pyridin-3-ylmethoxy)-benzoic acid methyl ester (288 mg, 1.0 mmol) in methanol (2 mL) and saturated aqueous ammonium chloride (1 mL) was added zinc dust (13.1 mg, 2.0 Mmol). After stirring for 12 hours, the reaction was diluted with 30 mL of ethyl acetate and washed with 30 mL of 10% aqueous sodium carbonate (2×30 mL), brine (1×30 mL), then dried (MgSO4), and filtered. The filtered solution was concentrated under reduced pressure to yield the desired product as a yellow solid (97% yield). 1H-NMR (400 MHz, CDCl3) δ 8.78 (s, 1H), 8.61 (d, 1H), 779 (d, 1H), 7.59 (m, 2H), 7.39 (m, 1H), 6.71 (d, 1H), 5.18 (s, 2H), 4.28 (br s, 2H), 3.85 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608618B2
Source datasetuspto-grants-2009_10
ORD IDord-7ffd535fa5ad4b02a32f8eb6647da3ff
Source noteuspto-grants-2009_10