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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607243Generated: October 25, 2026

4-Methyl-2-nitroaniline → (4-Benzyloxy-phenyl)-(4-methyl-2-nitro-phenyl)-amine

https://huagongshe.com/reaction/607243

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyl-2-nitroanilineHCID 6978—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-4-phenylmethoxybenzeneHCID 138835—
SolventO-XyleneHCID 7237—
Product(4-Benzyloxy-phenyl)-(4-methyl-2-nitro-phenyl)-amineHCID 66808397—

Reaction Steps

A mixture of 4-methyl-2-nitroaniline (1.006 g, 6.612 mmol), 4-benzyloxybromobenzene (5.794 g, 22.02 mmol), cuprous iodide (62.9 mg, 0.3306 mmol), potassium carbonate (0.914 g, 6.612 mmol) and anhydrous o-xylene (18 mL) was heated at 150° for 24 hours. Added additional cuprous iodide (30 mg) and heated an additional 6 hours at 160°. The reaction was cooled to room temperature and the solvent removed by rotary evaporation under vacuum. The residue was purified by silica gel flash chromatography using 1:1 methylene chloride/hexanes as eluent to afford the title compound as a red oil which slowly crystallized (1.23 g, 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915411B2
Source datasetuspto-grants-2011_03
ORD IDord-5a0fae2dbaef4e53adb89bd0f05912eb
Source noteuspto-grants-2011_03