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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190482Generated: October 29, 2026

Sodium Iodide → 2-(Benzyloxy)-4-fluoro-1-nitrobenzene

https://huagongshe.com/reaction/2190482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantBenzyl BromideHCID 7498—
Reactant5-Fluoro-2-nitrophenolHCID 9937—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
Product2-(Benzyloxy)-4-fluoro-1-nitrobenzeneHCID 11096908104.3%

Reaction Steps

To a solution of 5-fluoro-2-nitrophenol (8.05 g, 51.2 mmol) in acetone (100 mL) were added benzyl bromide (8.90 g, 52.0 mmol), potassium carbonate (11.0 g, 79.3 mmol) and sodium iodide (1.51 g, 10.1 mmol) at room temperature, and the mixture was heated under reflux for 2.5 hr. The reaction mixture was cooled to room temperature, the inorganic salt was filtered off, and the filtrate was concentrated. The residue was dissolved in ethyl acetate (150 mL), and the mixture was washed with water (150 mL×2) and saturated brine (100 mL), successively, and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure to give the title compound (13.2 g) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324395B2
Source datasetuspto-grants-2012_12
ORD IDord-82b7e558ea534399aeea46e986022777
Source noteuspto-grants-2012_12