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HRID 28282作成日:2026年10月24日

Acetic Anhydride → Ethyl 2-(formylamino)-alpha-oxo-4-thiazoleacetate

https://huagongshe.com/ja/reaction/28282

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物Potassium PermanganateHCID 516875—
反応物Ethyl 2-formamidothiazol-4-acetateHCID 688091—
反応物HCID 178470762HCID 178470762—
溶媒Acetic AcidHCID 176—
生成物Ethyl 2-(formylamino)-alpha-oxo-4-thiazoleacetateHCID 2733245—

反応手順

A mixture of manganous acetate tetrahydrate (120 g.), acetic acid (1000 ml) and acetic anhydride (100 ml.) was stirred for 20 minutes in an oil bath heated at 130° to 135° C., and to the mixture was added potassium permanganate (20 g.) over 5 minutes at 105° to 110° C. with stirring and then the mixture was further stirred for 30 minutes at 130° to 135° C. The mixture was cooled to room temperature, and to the mixture was added ethyl 2-(2-formylaminothiazol-4-yl)acetate, which can be represented as ethyl 2-(2-formylimino-2,3-dihydrothiazol-4-yl)acetate, (53.5 g.), and then the mixture was stirred for 15 hours at 38° to 40° C. under introduction of air at the rate of 6000 ml. per minute. After the reaction, the precipitates were collected by filtration. The precipitates were washed with acetic acid and water in turn and then dried to give ethyl 2-(2-formylaminothiazol-4-yl)glyoxylate, which can be represented as ethyl 2-(2-formylimino-2,3-dihydrothiazol-4-yl)glyoxylate, (41.5 g.), mp 232° to 233° C. (dec.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04225707
出典データセットuspto-grants-1980_09
ORD IDord-7ccb5fd1af4b433096c4032ff4abacd9
出典メモuspto-grants-1980_09