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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263436Generated: October 26, 2026

Nitrogen → 4-(4-Fluorophenoxy)-1-methyl-2-nitrobenzene

https://huagongshe.com/reaction/263436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
Reactant4-FluorophenolHCID 9732—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2-nitrotolueneHCID 123546—
SolventPyridineHCID 1049—
SolventDiethyl EtherHCID 3283—
Product4-(4-Fluorophenoxy)-1-methyl-2-nitrobenzeneHCID 353767363.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

4-Bromo-2-nitrotoluene (25.0g, 116 mmol), 4-fluorophenol (8.70g, 77.6 mmol), potassium carbonate (21.5g, 156 mmol) and pyridine (75 mL), were combined under N2 atmosphere and heated at 90° C. for 30 min. The reaction mixture was cooled to ambient temperature, CuO (15.4g, 194 mmol) was added under a stream of N2, and the resulting dark-brown suspension was heated at reflux for 17 hours. The reaction mixture was cooled to ambient temperature and diluted with ether. The solids were removed by filtration through celite. The ethereal solution was washed with 1.0M aqueous NaOH, 1.0M aqueous HCl and brine, dried over Na2SO4, filtered and concentrated in vacuo to give a dark-brown oil. The crude product was purified by chromatography on silica gel to give 2-nitro-4-(4-fluorophenoxy)-toluene (12.1 g, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05643922
Source datasetuspto-grants-1997_07
ORD IDord-2111e3ecfd044200b27d59782b961da2
Source noteuspto-grants-1997_07