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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107508Generated: November 2, 2026

Potassium Iodide → HCID 15381110, compound

https://huagongshe.com/reaction/1107508

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant2-BromophenolHCID 7244—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Chloro-2-butanoneHCID 20026—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 15381110HCID 1538111089%

Reaction Conditions

Temperature80 °C

Reaction Steps

60 g (347 mmol) of 2-bromophenol, 57.43 g (416 mmol) of potassium carbonate, 57 g (347 mmol) of potassium iodide, 600 ml of N,N-dimethylformamide and 4.34 g (416 mmol) of 3-chloro-2-butanone are introduced into a 1 liter three-necked flask equipped with a reflux condenser. The mixture is heated at 80° C. for 16 hours. 1500 ml of water are added and extraction is then carried out with ethyl acetate (3×400 ml). The organic phases are combined, washed with a molar sodium hydroxide solution (2×500 ml), dried over magnesium sulphate and concentrated. The residue is purified by chromatography on a silica column (elution solvent cyclohexane:ethyl acetate 9:1). 75.07 g (Yield: 89%) of 3-(2-bromophenoxy)-2-butanone (yellow oil) are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06060508
Source datasetuspto-grants-2000_05
ORD IDord-d09bc3a8c04440ce9b383930b56754a1
Source noteuspto-grants-2000_05