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HRID 34969생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물1,5-DibromopentaneHCID 8100—
반응물Sodium hydrideHCID 24758—
반응물3,4-Dichloro-2-propylphenolHCID 600360—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
용매HexamethylphosphoramideHCID 12679—
생성물5-(2-Propyl-3,4-dichlorophenoxy)pentyl bromideHCID 21297269—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04764521
출처 데이터셋uspto-grants-1988_08
ORD IDord-32c6fb647d2746f4aba904176db85cf6
출처 메모uspto-grants-1988_08