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HRID 2164643作成日:2026年10月25日

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

https://huagongshe.com/reaction/2164643

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物1,1-Dichloro-2,2-difluoroetheneHCID 6592—
反応物Sodium HydroxideHCID 14798—
反応物Phenol, 4-(4-(methylsulfonyl)phenoxy)-HCID 514882—
溶媒AcetonitrileHCID 6342—
生成物1-(2,2-Dichloro-1,1-difluoroethoxy)-4-(4-(methylsulfonyl)phenoxy)benzeneHCID 1307851989.4%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04505929
出典データセットuspto-grants-1985_03
ORD IDord-d14eb91a8c69406ab0fbbd650adcc03b
出典メモuspto-grants-1985_03