돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21408생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/21408

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl chloroacetateHCID 7751—
반응물Sodium hydrideHCID 24758—
반응물2-Benzylidenehydrazono-1-methoxycarbonylmethylimidazolidin-4-oneHCID 136040605—
용매WaterHCID 962—
용매ChloroformHCID 6212—
용매DimethylformamideHCID 6228—
생성물2-Benzylidenehydrazono-3-ethoxycarbonylmethyl-1-methoxycarbonylmethylimidazolidin-4-oneHCID 5412072144.4%

반응 조건

온도30 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05422360
출처 데이터셋uspto-grants-1995_06
ORD IDord-95f5bb33bf7440c88b09193ba4fb2a51
출처 메모uspto-grants-1995_06