戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 21408作成日:2026年10月26日

Ethyl chloroacetate → 2-Benzylidenehydrazono-3-ethoxycarbonylmethyl-1-methoxycarbonylmethylimidazolidin-4-one

https://huagongshe.com/reaction/21408

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl chloroacetateHCID 7751—
反応物Sodium hydrideHCID 24758—
反応物2-Benzylidenehydrazono-1-methoxycarbonylmethylimidazolidin-4-oneHCID 136040605—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
溶媒DimethylformamideHCID 6228—
生成物2-Benzylidenehydrazono-3-ethoxycarbonylmethyl-1-methoxycarbonylmethylimidazolidin-4-oneHCID 5412072144.4%

反応条件

温度30 °C

反応手順

In 20 ml of dimethylformamide (DMF) was suspended 96 mg of 60% sodium hydride under ice-cooling, 5 ml of a DMF solution of 548 mg of 2-benzylidenehydrazono-1-methoxycarbonylmethylimidazolidin-4-one was gradually added to the suspension. After stirring the mixture for one hour at 30° C., 254 mg of ethyl chloroacetate was gradually added dropwise thereto, followed by stirring for one hour at 80° C. After cooling the reaction mixture, water and chloroform was added thereto to distribute the mixture between water and chloroform, and the aqueous layer was further extracted three times with chloroform. The organic layer was combined with the extract, the mixture was dried over anhydrous magnesium sulfate, concentrated under reduced pressure, and the residue formed was recrystallized from a mixture of chloroform and n-hexane to obtain 320 mg of 2-benzylidenehydrazono-3-ethoxycarbonylmethyl-1-methoxycarbonylmethylimidazolidin-4-one.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05422360
出典データセットuspto-grants-1995_06
ORD IDord-95f5bb33bf7440c88b09193ba4fb2a51
出典メモuspto-grants-1995_06