Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 34969Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/34969

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium IodideHCID 4875—
Edukt1,5-DibromopentaneHCID 8100—
EduktSodium hydrideHCID 24758—
Edukt3,4-Dichloro-2-propylphenolHCID 600360—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelHexamethylphosphoramideHCID 12679—
Produkt5-(2-Propyl-3,4-dichlorophenoxy)pentyl bromideHCID 21297269—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04764521
Quelldatensatzuspto-grants-1988_08
ORD IDord-32c6fb647d2746f4aba904176db85cf6
Quellennotizuspto-grants-1988_08