関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzo(d)thiazol-2-amine | HCID 8706 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Sodium | HCID 5360545 | — |
| 反応物 | Potassium | HCID 5462222 | — |
| 反応物 | N-(2-Sulfanylphenyl)urea | HCID 23358470 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Diketene | HCID 12661 | — |
| 生成物 | 1-(1,3-Benzothiazol-2-yl)propan-2-one | HCID 320294 | 79.4% |
反応手順
The water-moist 2-mercaptophenylurea obtained according to European Pat. No. 0,039,483, Example 1, paragraph 1, by reacting 150 parts of 2-aminobenzothiazole with 150 parts of sodium hydroxide and working up the mixture with water, or an appropriate amount of the sodium or potassium salt of the said 2-mercaptophenylurea, is dissolved in 500 parts of 50% strength acetic acid, and 118 parts of diketene are then added dropwise in the course of 2 hours at 45° to 50° C. Stirring is continued for 1 hour, after which the mixture is heated to the reflux temperature and kept at a temperature of 95° C.-100° C. for 2 hours. It is then cooled to room temperature, and the precipitated 2-acetonylbenzothiazole of the formula ##STR13## is isolated by filtration and dried in vacuo at 60° C.-80° C. 151.7 parts of a product of melting point 118° C.-119° C. are obtained; this corresponds to a yield of 79.4%, based on 2-aminobenzothiazole employed.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04727154 |
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| 出典データセット | uspto-grants-1988_02 |
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| ORD ID | ord-3f4e5fd49dba41ce9980468ba16d9ddd |
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| 出典メモ | uspto-grants-1988_02 |
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