化工社化工社 化学情報印刷レポート · 研究参考用
Potassium Cyanide → 4-hydroxy-1H-1,2-benzisothiazole-1,1,3(2H)-trione
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Cyanide | HCID 9032 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Potassium | HCID 5462222 | — |
| 反応物 | 4-Methoxy-1H-1lambda~6~,2-benzothiazole-1,1,3(2H)-trione | HCID 14984051 | — |
| 反応物 | 3-Amino-4-methoxy-1,2-benzoisothiazole-1,1-dioxide | HCID 15567164 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 生成物 | 4-hydroxy-1H-1,2-benzisothiazole-1,1,3(2H)-trione | HCID 1486522 | 62% |
反応手順
2.5 gm (11.8 mmols) of 3-amino-4-methoxy-1,2-benzoisothiazole-1,1-dioxide were reacted with sodium hydroxide analogous to Example 5, and by subsequent acidification the reaction product was converted into 4-methoxy-1,2-benzoisothiazol-3(2H)-one-1,1-dioxide. The obtained compound, together with 650 mg (10 mmols) of potassium cyanide in dimethyl-sulfoxide, was heated at 180° C. for 3 hours. After addition of petroleum ether the potassium salt of the product was precipitated, and the precipitate was dissolved in water. After acidifying with aqueous hydrochloric acid, filtering and recrystallizing, 1.46 gm (62% of theory) of 4-hydroxy-1,2-benzoisothiazol-3(2H)-one-1,1-dioxide were obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04404230 |
| 出典データセット | uspto-grants-1983_09 |
| ORD ID | ord-9028caa34a404d9e8ab189188776807c |
| 出典メモ | uspto-grants-1983_09 |