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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275679Generated: October 26, 2026

Water → 1-Chloro-4-ethoxy-2-nitrobenzene

https://huagongshe.com/reaction/1275679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-3-nitrophenolHCID 69127—
SolventAcetoneHCID 180—
Product1-Chloro-4-ethoxy-2-nitrobenzeneHCID 24073494.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 4-chloro-3-nitrophenol (5.21 g, 30 mmol) in acetone (60 ml) were added ethyl iodide (5.94 g, 38 mmol) and potassium carbonate (4.53 g, 33 mmol), followed by stirring at 50° C. for 5 hours. After allowing to stand overnight, the reaction solution was poured into water and extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous sodium chloride solution and dried, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography [eluent; ethyl acetate-hexane (1:4)] to give the title compound (5.72 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06162832
Source datasetuspto-grants-2000_12
ORD IDord-f22391096a7a4478923087fc634a3098
Source noteuspto-grants-2000_12