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HRID 597421作成日:2026年10月24日

Hydrogen Peroxide → 4-((Chloromethyl)sulfonyl)phenol

https://huagongshe.com/ja/reaction/597421

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物WaterHCID 962—
反応物Sulfuric AcidHCID 1118—
反応物Acetic AnhydrideHCID 7918—
反応物4-(Methylthio)phenolHCID 14086—
反応物Sodium HydroxideHCID 14798—
反応物Sulfuryl chlorideHCID 24648—
触媒Sodium MolybdateHCID 61424—
溶媒1,2-DichloroethaneHCID 11—
生成物4-((Chloromethyl)sulfonyl)phenolHCID 1270762981%

反応条件

温度0 °C

反応手順

150 g (about 1.1 moles) of sulfuryl chloride were added dropwise, at 20° to 25° C, to a mixture of 140 g (1 mole) of 4-methylmercaptophenol, 880 g of ethylene chloride, 0.5 ml of concentrated sulfuric acid and 112 g (1.1 moles) of acetic anhydride. The mixture was stirred for a further hour at 40° to 45° C and a vigorous stream of air was then blown through the reaction solution for 10 minutes. After adding 0.5 g of sodium molybdate, 145 g of 50% strength hydrogen peroxide were added dropwise at 50° C. When the reaction had subsided, the batch was stirred for a further hour at 60° to 65° C; the excess peroxide was then destroyed with about 7 ml of 40% strength sodium bisulfite solution. Thereafter, a solution of 160 g (4 moles) of sodium hydroxide in 400 ml of water was added to the reaction mixture, which was kept below 50° C. The reaction of the mixture was then allowed to finish without cooling. The mixture was stirred for a further hour at 55° to 60° C and then cooled to 0° C, and the sodium phenolate which had precipitated was filtered off. It was dissolved in about 500 ml of water and aqueous hydrochloric acid was added until the mixture reacted strongly acid. After crystallization the product was filtered off and 167 g (81% of theory) of 4-chloromethylsulfonylphenol were obtained in the form of a colorless powder of melting point 110° C. ##STR33##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04013794
出典データセットuspto-grants-1977_03
ORD IDord-c7c24b3d25db4c51972963a4f59179e4
出典メモuspto-grants-1977_03