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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920805Generated: October 30, 2026

Iodoethane → HCID 58572422, compound

https://huagongshe.com/reaction/1920805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant1-(2-Bromo-3-hydroxyphenyl)ethanoneHCID 23216962—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 58572422HCID 5857242267%

Reaction Steps

Under a nitrogen atmosphere, 1-(2-bromo-3-hydroxy phenyl)ethanone (6.50 g, 30.2 mmol), which had been obtained in Reference example 3 (3c), and potassium carbonate (8.36 g, 60.5 mmol) were dissolved in N,N-dimethyl formamide (60 mL), and stirred at room temperature for 10 minutes. Subsequently, ethyl iodide (3.14 mL, 39.3 mmol) was added to the mixture, which was then further stirred for 21 hours. Ethyl acetate/hexane (1:1, V/V) and water were added to the reaction solution for fractionation, and the aqueous layer was extracted with ethyl acetate/hexane (1:1, V/V). The organic layers were combined, washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (hexane:ethyl acetate, 100:0-85:15, V/V) to give the title compound as a colorless oily substance (4.89 g, yield 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173631B2
Source datasetuspto-grants-2012_05
ORD IDord-a810acda1e1f46a8b78d389a642e62af
Source noteuspto-grants-2012_05