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HRID 28281作成日:2026年10月24日

Acetic Anhydride → Ethyl 2-formamidothiazol-4-acetate

https://huagongshe.com/ja/reaction/28281

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4-Thiazoleacetic acid, 2-amino-, ethyl esterHCID 104454—
反応物HCID 178470764HCID 178470764—
溶媒Formic AcidHCID 284—
生成物Ethyl 2-formamidothiazol-4-acetateHCID 688091—

反応手順

To acetic anhydride (384 ml.) was added dropwise formic acid (169.2 ml.) over 15 to 20 minutes under cooling below 35° C., and the mixture was stirred for 1 hour at 55° to 60° C. To the mixture was added ethyl 2-(2-aminothiazol-4-yl)acetate, which can be represented as ethyl 2-(2-imino-2,3-dihydrothiazol-4-yl)acetate, (506 g.) over 15 to 20 minutes under ice-cooling and stirring, and then the mixture was stirred for 1 hour at room temperature. After the reaction, the solvents were distilled off. To the residue was added diisopropyl ether (2500 ml.), and the mixture was stirred for 1 hour at room temperature. The precipitates were collected by filtration, washed with diisopropyl ether and then dried to give ethyl 2-(2-formylaminothiazol-4-yl)acetate, which can be represented as ethyl 2-(2-formylimino-2,3-dihydrothiazol-4-yl)acetate, (451.6 g.), mp 125° to 126° C. The remaining filtrate was concentrated, and the residue was washed with diisopropyl ether (500 ml.) and then dried to give further the same object compound (78.5 g.).

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-ade6e4231f984fbe822c52863510b16d
出典メモuspto-grants-1980_09