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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518812Generated: October 31, 2026

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

https://huagongshe.com/reaction/518812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
Reactant5-Fluoro-2-nitrophenolHCID 9937—
ReactantCesium carbonateHCID 10796—
SolventDimethylformamideHCID 6228—
Product4-Fluoro-1-nitro-2-(propan-2-yloxy)benzeneHCID 10631832—

Reaction Steps

A mixture of 18.0 g of 5-fluoro-2-nitrophenol, 29.0 g of caesium carbonate and 13.7 ml of 2-iodopropane in 119 ml of DMF is stirred at ambient temperature overnight. The mixture is concentrated under vacuum and the residue is taken up with 250 ml of water and extracted twice with 250 ml of ethyl acetate. The organic phases are washed twice with 200 ml of a saturated sodium chloride solution, dried over magnesium sulfate and concentrated under vacuum, so as to obtain 17 g of crude product. The crude product is purified on 400 g of silica, elution being carried out with cyclohexane/ethyl acetate (95/5), so as to obtain 13.0 g of 4-fluoro-1-nitro-2-(propan-2-yloxy)benzene in the form of a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115140B2
Source datasetuspto-grants-2015_08
ORD IDord-f16f2dd567044c47bcb1f2b9f5f1cc1e
Source noteuspto-grants-2015_08