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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2164643생성일: 2026년 10월 24일

Water → 1-(2,2-Dichloro-1,1-difluoroethoxy)-4-(4-(methylsulfonyl)phenoxy)benzene

https://huagongshe.com/ko/reaction/2164643

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1,1-Dichloro-2,2-difluoroetheneHCID 6592—
반응물Sodium HydroxideHCID 14798—
반응물Phenol, 4-(4-(methylsulfonyl)phenoxy)-HCID 514882—
용매AcetonitrileHCID 6342—
생성물1-(2,2-Dichloro-1,1-difluoroethoxy)-4-(4-(methylsulfonyl)phenoxy)benzeneHCID 1307851989.4%

반응 단계

To a solution of 5.29 g (0.0200 mole) of 4-(4-(methylsulfonyl)phenoxy)phenol (Example 21) in 100 ml of acetonitrile was added 0.80 g (0.0200 mole) of NaOH. The mixture was stirred at room temperature for 1 hr and then cooled to 3° C. in an ice bath. To the cold slurry was slowly added 4.0 g (0.0300 mole) of 1,1-difluoro-2,2-dichloroethylene dissolved in 15 ml of acetonitrile and the reaction mixture stirred at 3°-5° C. for 3 hrs. To the cold mixture 150 ml of water was added which resulted in the product precipitating as an oil. The product was extracted from the mixture with CH2Cl2. The organic layer was washed with water, dried (Na2SO4) and solvent removed in vacuo, which gave 7.1 g (89.4% yield) of product. Purification was accomplished by column chromatography using silica gel as the support and chloroform as the eluent, which afforded purified 1 -(2,2-dichloro-1,1-difluoroethoxy)-4-(4-(methylsulfonyl)phenoxy)benzene, mp 67°-70° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04505929
출처 데이터셋uspto-grants-1985_03
ORD IDord-d14eb91a8c69406ab0fbbd650adcc03b
출처 메모uspto-grants-1985_03