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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl chloroacetate | HCID 7751 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 2-Benzylidenehydrazono-1-methoxycarbonylmethylimidazolidin-4-one | HCID 136040605 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-Benzylidenehydrazono-3-ethoxycarbonylmethyl-1-methoxycarbonylmethylimidazolidin-4-one | HCID 54120721 | 44.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05422360 |
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| 출처 데이터셋 | uspto-grants-1995_06 |
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| ORD ID | ord-95f5bb33bf7440c88b09193ba4fb2a51 |
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| 출처 메모 | uspto-grants-1995_06 |
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