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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 436657생성일: 2026년 10월 23일

Potassium Iodide → 4-Cyclopropoxybenzoic acid

https://huagongshe.com/ko/reaction/436657

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물EthylparabenHCID 8434—
반응물Potassium CarbonateHCID 11430—
반응물BromocyclopropaneHCID 78037—
반응물Ethyl 4-(cyclopropyloxy)benzoateHCID 21453006—
용매DimethylformamideHCID 6228—
생성물4-Cyclopropoxybenzoic acidHCID 21452864—

반응 단계

The intermediate 4-cyclopropyloxybenzoic acid was prepared as follows: A 66.5 g. portion of ethyl 4-hydroxybenzoate was dissolved in 800 ml. of dimethylformamide and to the solution was added 83.0 g. of anhydrous potassium carbonate and 5 g. of potassium iodide. To the resulting stirred suspension was added 60.5 g. of cyclopropyl bromide. The stirred reaction mixture was refluxed for 6 days and the hot reaction mixture was filtered to remove the inorganic solids which were washed well with dimethylformamide. The combined filtrate and dimethylformamide washings were evaporated in vacuo and the remaining liquid-solid residue was taken up in a mixture of 500 ml. of water and 500 ml. of ether. The resulting mixture was shaken well and the layers were separated. The aqueous layer was extracted with 200 ml. of ether. The combined ether solutions were washed successively with two 250 ml. portions of aqueous potassium hydroxide solution, next with 200 ml. 0.5N hydrochloric acid and then with two 100 ml. portions of water. The ether solution was dried over anhydrous magnesium sulfate and the ether removed in vacuo to yield, as an amber liquid, 36.2 g. of ethyl 4-cyclopropyloxy-benzoate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04009208
출처 데이터셋uspto-grants-1977_02
ORD IDord-9958e0c525e74815a94420815c7b6e1b
출처 메모uspto-grants-1977_02