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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188896Generated: November 2, 2026

Isopropyl iodide → 4-Fluoro-1-nitro-2-(propan-2-yloxy)benzene

https://huagongshe.com/reaction/1188896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
Reactant5-Fluoro-2-nitrophenolHCID 9937—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
Product4-Fluoro-1-nitro-2-(propan-2-yloxy)benzeneHCID 1063183265.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 5-fluoro-2-nitrophenol (91.0 g), 2-iodopropane (103.4 g), potassium carbonate (146 g) and N,N-dimethylformamide (600 mL) was stirred at 50° C. for 3.5 h. The mixture was concentrated under reduced pressure and water was added to the residue. The mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate, filtered and concentrated. The residue was purified by basic silica gel column chromatography (ethyl acetate/hexane=0/100 to 30/70, volume ratio) to give the title compound (75.4 g, 65%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673942B2
Source datasetuspto-grants-2014_03
ORD IDord-a0121e791f604750b19ca7a6c285a8c3
Source noteuspto-grants-2014_03