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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34967Generated: October 25, 2026

Potassium Iodide → 6-(2-Propyl-3,4-dichlorophenoxy)hexanoic acid

https://huagongshe.com/reaction/34967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant6-Bromohexanoic acidHCID 20210—
ReactantSodium hydrideHCID 24758—
Reactant3,4-Dichloro-2-propylphenolHCID 600360—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventHexamethylphosphoramideHCID 12679—
Product6-(2-Propyl-3,4-dichlorophenoxy)hexanoic acidHCID 14233046—

Reaction Steps

To a solution of 1.1 g. of 2-propyl-3,4-dichlorophenol in 30 ml. of tetrahydrofuran and 30 ml. of hexamethylphosphoramide were added 4.1 g. of 6bromohexanoic acid. To the solution were then added 1.3 g. of a 50% oil dispersion of sodium hydride. A catalytic amount of potassium iodide was added and the reaction was stirred under a nitrogen atmosphere at 60°-70° C. overnight. The reaction was cooled to room temperature and ethyl acetate and water were added. The solution was evaporated to dryness. Fresh ethyl acetate and water were added and the layers were separated. Fresh ethyl acetate was added to the aqueous layer and the aqueous layer was adjusted to pH 2. The layers were separated and the organic layer was washed with a saturated sodium chloride solution. The organic layer was then filtered through sodium sulfate and evaporated to dryness. The resulting residue was extracted with hexane and evaporated to dryness to afford 500 mg. of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04764521
Source datasetuspto-grants-1988_08
ORD IDord-e251a63eb2424cdea2c6965031dc78a9
Source noteuspto-grants-1988_08