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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 325831생성일: 2026년 10월 25일

Dimethyl Sulfoxide → 2-[5-(2-Cyano-4-fluorophenoxy)-2-methylthiophenoxy]propionamide

https://huagongshe.com/reaction/325831

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물WaterHCID 962—
반응물2-BromopropanamideHCID 101118—
반응물5-(2-Cyano-4-fluorophenoxy) 2-(methylthio)phenolHCID 20462849—
용매Ethyl acetate hexaneHCID 21226206—
생성물2-[5-(2-Cyano-4-fluorophenoxy)-2-methylthiophenoxy]propionamideHCID 131713486—

반응 단계

5-(2-Cyano-4-fluorophenoxy)-2-(methylthio)phenol (0.05 mole) potassium carbonate (0.2 mole), 2-bromopropionamide (0.08 mole) and dimethylsulfoxide (200 ml) are charged into a 500 ml glass reaction flask equipped with a mechanical stirrer. The reaction mixture is stirred at room temperature for a period of about 8 hours. After this time the mixture is poured into 500 ml of water. The resulting mixture is extracted three times with 100 ml portions of methylene chloride. The extracts are then combined, washed with water and thereafter dried. The dried solution is then stripped of solvent under reduced pressure to leave a residue. The residue is subjected to chromatography using a clay column and hexane/ethyl acetate mixtures as the eluant. The fractions containing the product are combined and stripped of solvent to yield the desired product 2-[5-(2-cyano-4-fluorophenoxy)-2-methylthiophenoxy]propionamide as the residue.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04443248
출처 데이터셋uspto-grants-1984_04
ORD IDord-558b3d313b6544dda8e9439e419a4d5b
출처 메모uspto-grants-1984_04