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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696719Generated: November 1, 2026

4-Methoxy-2-nitroaniline → HCID 59004212, compound

https://huagongshe.com/reaction/1696719

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxy-2-nitroanilineHCID 66793—
Reactant5-Bromo-2-nitropyridineHCID 817620—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
ProductHCID 59004212HCID 590042127%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 4-methoxy-2-nitrobenzenamine (8 g, 47.62 mmol), 5-bromo-2-nitropyridine (7.2 g, 35.47 mmol), and potassium 2-methylpropan-2-olate (6 g, 53.57 mmol) in DMF (180 ml) was allowed to stir for 5 hours at 30° C. and overnight at 60° C. After being cooled down to room temperature, the reaction mixture was quenched by the addition of H2O (200 mL) and the resulting solution was extracted three times with 400 ml of EtOAc, washed with 200 ml of H2O and 200 ml of brine. The mixture was dried and concentrated under reduced pressure. The crude material such obtained was purified by solvating gas chromatography (SGC) using 1:10-1:5 EtOAc/PE as eluents to provide 800 mg (5%) of (5-Bromo-pyridin-2-yl)-(4-methoxy-2-nitro-phenyl)-amine (z) as a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163777B2
Source datasetuspto-grants-2012_04
ORD IDord-bf7ca1fccf3e430f8f3002961e8864dd
Source noteuspto-grants-2012_04