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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129872Generated: October 25, 2026

3,4-Dichlorophenol → 2-(2-Nitro-4-trifluoromethylphenoxy)-4,5-dichlorobenzene

https://huagongshe.com/reaction/129872

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DichlorophenolHCID 7258—
Reactant4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotolueneHCID 8462—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
Product2-(2-Nitro-4-trifluoromethylphenoxy)-4,5-dichlorobenzeneHCID 1343009—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 3,4-dichlorophenol (25 gram (hereinafter g), 0.153 mol), 4-chloro-3-nitrobenzo-trifluoride (52 g, 0.23 mol) and potassium carbonate (63 g, 0.459 mol) in dimethylformamide (450 mL)was stirred under argon at 120° C. for 24 h. The reaction mixture was filtered and the filtrate evaporated. The residue was dissolved in ethyl acetate, washed with water, brine, dried over anhydrous magnesium sulfate, filtered and evaporated. The residue was flash chromatographed (silica gel, methylene chloride/hexane), to give the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05470882
Source datasetuspto-grants-1995_11
ORD IDord-2c6a3196267a4fda9525cf2daac82a75
Source noteuspto-grants-1995_11