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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583171Generated: October 30, 2026

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

https://huagongshe.com/reaction/583171

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4-nitroanisoleHCID 78870—
CatalystIronHCID 23925—
SolventAcetic acid--water (1/1)HCID 21899381—
Product3-Bromo-4-methoxyanilineHCID 96108386%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 670 mg (2.9 mmol) of 2-bromo-4-nitroanisole and 1.20 g (21.1. mmol) of iron powder in 10 mL of 1:1 v/v HOAc/H2O was heated at 80° C. for 1.5 h. The mixture was cooled and filtered onto a pad of Celite. The flask and filtered solids were rinsed with 100 mL of EtOAc and 100 mL of H2O. The filtrate was transfered to a separatory fumel and the layers were separated. The organic layer was washed with 50 mL of sat'd NaHCO3, 50 mL sat'd NaCl, dried over MgSO4 and concentrated in vacuo. Flash chromatography on 25 g of silica gel using 3:2 v/v hexanes/ether as the eluant afforded 504 mg (86%) of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05929094
Source datasetuspto-grants-1999_07
ORD IDord-a0c30345ef4c419390b9482b190cf44b
Source noteuspto-grants-1999_07