関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 5-Methyl-6-phenylsulphonyl-1,3-benzodioxole-2-carboxylic acid ethyl ester | HCID 53963760 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 5-Methyl-6-phenylsulphonyl-1,3-benzodioxole-2-carboxylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04600709 |
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| 出典データセット | uspto-grants-1986_07 |
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| ORD ID | ord-6e4c1cff1cb246fb8c87c842d9cd1432 |
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| 出典メモ | uspto-grants-1986_07 |
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