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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34969Generated: October 25, 2026

Potassium Iodide → 5-(2-Propyl-3,4-dichlorophenoxy)pentyl bromide

https://huagongshe.com/reaction/34969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1,5-DibromopentaneHCID 8100—
ReactantSodium hydrideHCID 24758—
Reactant3,4-Dichloro-2-propylphenolHCID 600360—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventHexamethylphosphoramideHCID 12679—
Product5-(2-Propyl-3,4-dichlorophenoxy)pentyl bromideHCID 21297269—

Reaction Steps

To a solution of 3.12 g. of 2-propyl-3,4dichlorophenol in 30 ml. of dry tetrahydrofuran and 30 ml. of dry hexamethylphosphoramide were added 0.72 g. of a 50% sodium hydride dispersion in oil. Two milliliters of 1,5-dibromopentane were then added followed by a catalytic amount of potassium iodide. The reaction was stirred overnight under a nitrogen atmosphere at 60°-70° C. The reaction was then cooled to room temperature, ethyl acetate and water were added, and the solution was evaporated to dryness. Ethyl acetate and water were added to the residue and the layers were separated. The ethyl acetate layer was washed with dilute acid to remove residual hexamethylphosphoramide. The ethyl acetate was then washed with a saturated sodium chloride solution, filtered through sodium sulfate, and evaporated to dryness. The residue was purified by high pressure liquid chromatography to provide 1.6 g. of the desired bromo intermediate. NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04764521
Source datasetuspto-grants-1988_08
ORD IDord-32c6fb647d2746f4aba904176db85cf6
Source noteuspto-grants-1988_08