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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13430생성일: 2026년 10월 24일

Dimethyl Sulfoxide → 6-(Methylsulfonyl)pyridin-3-ol

https://huagongshe.com/ko/reaction/13430

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물Ethyl AcetateHCID 8857—
반응물Potassium AcetateHCID 517044—
반응물5-Bromo-2-methanesulfonylpyridineHCID 13433424—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물6-(Methylsulfonyl)pyridin-3-olHCID 23145196—

반응 조건

온도80 °C

반응 단계

6.6 g of bis(pinacolate)diboron, 5.9 g of potassium acetate and 980 mg of (1,1′-bis(diphenylphosphino)ferrocene)dichloropalladium(II) dichloromethane complex were added to a dimethylsulfoxide (80 ml) solution of 4.72 g of 3-bromo-6-methanesulfonyl-pyridine, and the reaction liquid was stirred at 80° C. for 2 hours. Ethyl acetate and water were added to the reaction liquid, the insoluble substance was removed through filtration through Celite, and the organic layer was separated. The organic layer was washed with water and saturated saline, and dried with anhydrous magnesium sulfate, and the solvent was evaporated away under reduced pressure. 60 ml of aqueous 5 N sodium hydroxide solution and 30 ml of aqueous 30% hydrogen peroxide solution were added to a tetrahydrofuran (200 ml) solution of the resulting residue at 0° C., and the reaction liquid was stirred overnight at room temperature. The reaction liquid was diluted with diethyl ether, and washed with water. The aqueous layer was made acidic with 5 N hydrochloric acid, and extracted with ethyl acetate. The organic layer was dried with anhydrous magnesium sulfate, and the solvent was evaporated away under reduced pressure. The resulting residue was washed with a mixed solvent of chloroform and hexane to obtain the entitled compound as a brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728025B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-8cb018741c2b4d8d9221b51b787d6e50
출처 메모uspto-grants-2010_06