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HRID 745788作成日:2026年10月27日

Hydrochloric Acid → 5-Methyl-6-phenylsulphonyl-1,3-benzodioxole-2-carboxylic acid

https://huagongshe.com/reaction/745788

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium HydroxideHCID 14798—
反応物5-Methyl-6-phenylsulphonyl-1,3-benzodioxole-2-carboxylic acid ethyl esterHCID 53963760—
溶媒MethanolHCID 887—
生成物5-Methyl-6-phenylsulphonyl-1,3-benzodioxole-2-carboxylic acidHCID 23312092—

反応手順

8.6 g (24.7 mmol) of 5-methyl-6-phenylsulphonyl-1,3-benzodioxole-2-carboxylic acid ethyl ester are suspended in 37 ml of methanol. 37 ml of 1N sodium hydroxide solution are then slowly added at room temperature, the starting material soon dissolving. After one hour the reaction mixture is cooled, concentrated hydrochloric acid is added and the whole is extracted three times with ethyl acetate. The combined organic phases are washed with water and then with a saturated sodium chloride solution, dried over sodium sulphate and concentrated by evaporation. 50 ml of methylene chloride are added to the yellow oil remaining, and the whole is stirred until crystallisation occurs. The filtered crystals are recrystallised from a small amount of 1,2-dichloroethane, yielding 5-methyl-6-phenylsulphonyl-1,3-benzodioxole-2-carboxylic acid in the form of white crystals having a melting point of 169°-171°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04600709
出典データセットuspto-grants-1986_07
ORD IDord-6e4c1cff1cb246fb8c87c842d9cd1432
出典メモuspto-grants-1986_07