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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448379Generated: October 30, 2026

Isopropyl iodide → 4-Fluoro-2-isopropoxy-1-nitrobenzene

https://huagongshe.com/reaction/448379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
Reactant5-Fluoro-2-nitrophenolHCID 9937—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
Product4-Fluoro-2-isopropoxy-1-nitrobenzeneHCID 10631832—

Reaction Steps

A mixture of 5-fluoro-2-nitrophenol (2.5 g, 15.9 mmol), 2-iodopropane (5.4 g, 31.8 mmol), and potassium carbonate (4.2 g, 39.8 mmol) in acetone (40 mL) was heated to reflux for 16 hours. The mixture was cooled and evaporated under vacuum, and the residue was partitioned between ethyl acetate (100 mL) and water (150 mL), and the aqueous phase was extracted with ethyl acetate (100 mL). The combined organic layers were washed with water (3×150 mL), dried (MgSO4), and evaporated, providing 3.2 g, in quantitative yield; 1H NMR (CDCl3) δ 1.42 (d, J=6.0 Hz, 6H), 4.63 (septet, J=6.0 Hz, 6H), 6.64-6.72 (m, 1H), 6.76 (dd, J=9.8 Hz, J=2.5 Hz, 1H), 7.88 (dd, J=8.9 Hz, J=6.1 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481568B2
Source datasetuspto-grants-2013_07
ORD IDord-7b6241e8aca64547b4170d1c0a60b6d5
Source noteuspto-grants-2013_07