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HRID 569782作成日:2026年10月26日

1,3-Diethyl 2-oxopropanedioate → hydroxy [2-[4-(1H-imidazol-1-yl)-phenyl]-2-oxoethyl]propanedioic acid diethyl ester

https://huagongshe.com/reaction/569782

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-Diethyl 2-oxopropanedioateHCID 69105—
反応物1-(4-(1H-Imidazol-1-yl)phenyl)ethanoneHCID 82316—
溶媒EthanolHCID 702—
生成物hydroxy [2-[4-(1H-imidazol-1-yl)-phenyl]-2-oxoethyl]propanedioic acid diethyl esterHCID 1409946037.2%

反応手順

A mixture of diethylketomalonate (87.08 g, 0.50 mole) and 4-(imidazol-1-yl)acetophenone (93.1 g, 0.50 mole) is warmed to 95°-100° C. with stirring for three hours. During this time, the original tan slurry is transformed into a black syrup. At the end of three hours, anhydrous ethanol (130 ml) is added with stirring, resulting in a black solution. This solution is cooled to room temperature, an aliquot is removed and scratched to induce crystallization, and the crystals thus obtained returned to the cool solution. Upon standing overnight at 8° C., the solution forms a solid mass, which is suspended in absolute ethanol (100 ml) and filtered to obtain a brownish solid, which is dried at 43° in a vacuum oven for four hours to yield 67 g hydroxy [2-[4-(1H-imidazol-1-yl)-phenyl]-2-oxoethyl]propanedioic acid diethyl ester. Material thus obtained is suitable for use without additional purification, however, it can be recrystallized from methanol to give pure product, mp 155°-156° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04734415
出典データセットuspto-grants-1988_03
ORD IDord-a6d889bdde874485be5ea9b902cc02eb
出典メモuspto-grants-1988_03