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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34967생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물6-Bromohexanoic acidHCID 20210—
반응물Sodium hydrideHCID 24758—
반응물3,4-Dichloro-2-propylphenolHCID 600360—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
용매HexamethylphosphoramideHCID 12679—
생성물6-(2-Propyl-3,4-dichlorophenoxy)hexanoic acidHCID 14233046—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04764521
출처 데이터셋uspto-grants-1988_08
ORD IDord-e251a63eb2424cdea2c6965031dc78a9
출처 메모uspto-grants-1988_08