関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Dibromoacetic Acid | HCID 12433 | — |
| 反応物 | 4-(2-Chlorophenylsulphonyl)-5-methyl-1,2-benzenediol | HCID 23312099 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 5-(2-Chlorophenylsulphonyl)-6-methyl-1,3-benzodioxole-2-carboxylic acid | HCID 23312095 | — |
反応手順
23 g (77 mmol) of 4-(2-chlorophenylsulphonyl)-5-methyl-1,2-benzenediol are added to a finely particulate suspension of 50.9 g (385 mmol) of freshly calcined potassium carbonate in 180 ml of dry dimethylformamide and there is added dropwise thereto, in the course of 15 minutes, a solution of 8.50 g (39 mmol) of dibromoacetic acid in 80 ml of dimethylformamide. The mixture is then stirred for 15 hours at 80°. Subsequently, the reaction mixture is poured onto ice and adjusted to pH 1-2 with concentrated hydrochloric acid. The aqueous phase is extracted once more with ethyl acetate. The combined organic phases are washed with water and saturated sodium chloride solution, dried with sodium sulphate and concentrated by evaporation. The resulting brown oil is stirred with 150 ml of ethyl acetate at 0° until crystallisation occurs. The crude 5-(2-chlorophenylsulphonyl)-6-methyl-1,3-benzodioxole-2-carboxylic acid so obtained is recrystallised twice from acetonitrile, resulting in the form of sand-coloured crystals having a melting point of 211°-213.5°.
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-2bba5278dfe74136921fe1189a35daf6 |
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| 出典メモ | uspto-grants-1986_07 |
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