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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107276Generated: October 31, 2026

2-Bromo-4-nitroanisole → 3-Bromo-4-methoxyaniline

https://huagongshe.com/reaction/1107276

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4-nitroanisoleHCID 78870—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product3-Bromo-4-methoxyanilineHCID 961083—

Reaction Steps

A mixture 2-bromo-4-nitroanisole (15 g, 64.6 mmol) and iron powder (27.3 g, 0.49 mol) in water (100 ml) and glacial acetic acid (25 ml) was stirred at reflux for 2 hours. The mixture was allowed to cool to ambient temperature and filtered through a pad of Hyflo™ (washed with 25% acetic acid/water). The filtrate was extracted with ethyl acetate (2×250 ml) and the organic layer was dried over sodium sulphate. Removal of the solvent in vacuo left an oil which was chromatographed on silica eluting with 40% ethyl acetate/hexane giving the title compound as a brown solid (10.32 g, 79%). Mass Spec ES+ 202 M+1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06060469
Source datasetuspto-grants-2000_05
ORD IDord-171177a952b046baba213084eeb57670
Source noteuspto-grants-2000_05