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Water → 1,2-Benzisothiazol-3(2H)-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Sulfuryl chloride | HCID 24648 | — |
| 反応物 | 2-(Methylthio)benzonitrile | HCID 138781 | — |
| 溶媒 | Chlorobenzene | HCID 7964 | — |
| 生成物 | 1,2-Benzisothiazol-3(2H)-one | HCID 17520 | 95.9% |
反応手順
To a 500 ml four-necked flask equipped with a stirrer, a thermometer, and a condenser, 29.8 g (0.2 mol) of 2-(methylthio)benzonitrile, 100 g of monochlorobenzene, and 4.32 g (0.24 mol) of water were added. To the flask, 29.7 g (0.22 mol) of sulfuryl chloride was added with stirring at a temperature of from 5° to 15° C., heated to a temperature of from 70° to 80° C., and allowed to react for 1 hour. After the completion of the reaction, the reaction mixture was cooled to room temperature to precipitate white crystals. The white crystals were washed with monochlorobenzene, and dried to give 29.0 g of 1,2-benzisothiazol-3-one (melting point: 157° to 158° C.). The yield of the product was 96% against the starting 2-(methylthio)benzonitrile.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05633384 |
| 出典データセット | uspto-grants-1997_05 |
| ORD ID | ord-ec3883f08a9549f0b176e5b6eb825c8b |
| 出典メモ | uspto-grants-1997_05 |