戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 587020作成日:2026年10月27日

Ethyl bromopyruvate → Ethyl 2-methyl-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/587020

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl bromopyruvateHCID 66144—
反応物Sodium BicarbonateHCID 516892—
反応物ThioacetamideHCID 2723949—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 2-methyl-1,3-thiazole-4-carboxylateHCID 29335347.9%

反応手順

To a solution of thioacetamide (11.9 g) in tetrahydrofuran (600 ml) was added sodium hydrogen carbonate (66.4 g), followed by addition of 80% ethyl bromopyruvate (50.0 g) at 0° C. The mixture was stirred overnight, the insolubles were filtered using Celite and the solvent was evaporated under reduced pressure. The resulting residue was dissolved in tetrahydrofuran (170 ml), and to the solution was added dropwise trifluoroacetic anhydride (170 ml) at 0° C., and the mixture was stirred at room temperature for 1 hour. To the mixture was added dropwise pyridine (200 ml) at 0° C., and the mixture was stirred at room temperature for 3 hours. The solvent was evaporated under reduced pressure, to the mixture was added ethyl acetate, and the mixture was washed with saturated sodium hydrogen carbonate solution and further with saturated brine and dried with magnesium sulfate. The solvent was evaporated under reduced pressure, and the resulting residue was purified with silica gel column chromatography (hexane:ethyl acetate=2:1) to give ethyl 2-methylthiazole-4-carboxylate (13.0 g) as brown crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06936602B1
出典データセットuspto-grants-2005_08
ORD IDord-2df540d858d04c5ab7e61e69aa7b6f52
出典メモuspto-grants-2005_08