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HRID 34967Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/34967

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
Edukt6-Bromohexanoic acidHCID 20210—
EduktSodium hydrideHCID 24758—
Edukt3,4-Dichloro-2-propylphenolHCID 600360—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelHexamethylphosphoramideHCID 12679—
Produkt6-(2-Propyl-3,4-dichlorophenoxy)hexanoic acidHCID 14233046—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04764521
Quelldatensatzuspto-grants-1988_08
ORD IDord-e251a63eb2424cdea2c6965031dc78a9
Quellennotizuspto-grants-1988_08