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HRID 4702作成日:2026年10月24日

Benzo(d)thiazol-2-amine → 1-(1,3-Benzothiazol-2-yl)propan-2-one

https://huagongshe.com/ja/reaction/4702

反応式

関与物質

役割名称HCID仕込み量
反応物Benzo(d)thiazol-2-amineHCID 8706—
反応物Sodium HydroxideHCID 14798—
反応物SodiumHCID 5360545—
反応物PotassiumHCID 5462222—
反応物N-(2-Sulfanylphenyl)ureaHCID 23358470—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
溶媒DiketeneHCID 12661—
生成物1-(1,3-Benzothiazol-2-yl)propan-2-oneHCID 32029479.4%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04727154
出典データセットuspto-grants-1988_02
ORD IDord-3f4e5fd49dba41ce9980468ba16d9ddd
出典メモuspto-grants-1988_02