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HRID 30637作成日:2026年10月24日

Ethyl bromopyruvate → Ethyl 2-(4-nitrobenzyl)-1,3-thiazole-4-carboxylate

https://huagongshe.com/ja/reaction/30637

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2-(4-Nitrophenyl)thioacetamideHCID 2777337—
溶媒EthanolHCID 702—
生成物Ethyl 2-(4-nitrobenzyl)-1,3-thiazole-4-carboxylateHCID 69207729—

反応手順

A mixture of 2-(4-nitrophenyl)ethanethioamide (1.50 g), ethyl bromopyruvate (1.64 g) and ethanol (50 mL) was heated under reflux for 30 min. The reaction mixture was concentrated, and ethyl acetate was added to the residue. The mixture was washed successively with saturated aqueous sodium hydrogen carbonate and saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography, and ethyl 2-(4-nitrobenzyl)-1,3-thiazole-4-carboxylate was obtained as pale-yellow crystals (1.79 g, yield 81%) from a fraction eluted with hexane-ethyl acetate (1:1, v/v). Recrystallization thereof from ethyl acetate-hexane gave pale-yellow prism crystals. melting point: 122-123° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423159B2
出典データセットuspto-grants-2008_09
ORD IDord-106a5dcb434146ce9a99300627addbf3
出典メモuspto-grants-2008_09