関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Methylbenzothiazole | HCID 8446 | — |
| 反応物 | Chlorosulfonic acid | HCID 24638 | — |
| 生成物 | 2-Methylbenzo[d]thiazole-4-sulfonyl chloride | HCID 13824425 | — |
反応手順
2-Methylbenzothiazole (50 g) was added in a slow, dropwise manner to 86 mL of chlorosulfonic acid at room temperature. When the addition was complete, the dark reaction mixture was heated at 140°-145° C. for about 3 hours. The solution was allowed to cool and was slowly added to a large excess of ice. Insoluble solids were removed by filtration and the aqueous layer was extracted with benzene. Drying and evaporation of the solvent gave an off-white solid which was shown by 1H NMR analysis to consist of a mixture of sulfonyl chlorides, presumably the 4-, 6-, and 7-isomers. This crude material was recrystallized three times from hexane to remove the 6-isomer as a white solid, m.p. 100°-102° C. The combined mother liquors were concentrated to give a dark yellow oil which was carried on to the next step without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04643759 |
|---|
| 出典データセット | uspto-grants-1987_02 |
|---|
| ORD ID | ord-3fe9f9e2bb2d48fa8c1ec81089209487 |
|---|
| 出典メモ | uspto-grants-1987_02 |
|---|