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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803124Generated: October 25, 2026

1-(2-methoxy-4-nitrophenyl)-3-methyl-1H-1,2,4-triazole → 3-Methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)aniline

https://huagongshe.com/reaction/1803124

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-methoxy-4-nitrophenyl)-3-methyl-1H-1,2,4-triazoleHCID 59577788—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-Methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)anilineHCID 5957781894.1%

Reaction Steps

Step F (2): 10% Palladium on carbon (1.2 g) was added under an atmosphere of nitrogen to a chilled (ice-water bath) solution of 1-(2-methoxy-4-nitrophenyl)-3-methyl-1H-1,2,4-triazole (3.7 g, 12.7 mmol) dissolved in methanol (250 mL). The flask was repeated evacuated and flushed with hydrogen gas (double balloon). The resulting mixture was allowed to warm to rt and left to stir for 18 h under the hydrogen atmosphere. Purged with nitrogen gas. Filtered the crude reaction mixture through a short diatomaceous earth (Celite®) plug. Rinsed reaction vessel and plug with methanol. Concentrated filtrate in vacuo. Dried residue on high vacuum overnight to afford 3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)aniline (2.44 g, 94% yield) as a reddish solid. LC-MS (M+H)+ 205.2. 1H NMR (500 MHz, chloroform-d) δ ppm 8.35 (s, 1 H) 7.36 (d, J=8.55 Hz, 1 H) 6.29-6.34 (m, 2 H) 3.80 (s, 3 H) 2.46 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349880B2
Source datasetuspto-grants-2013_01
ORD IDord-568b323d659e48589de0d015cdd8d2db
Source noteuspto-grants-2013_01