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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Ethyl chloroacetate | HCID 7751 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 2-Benzylidenehydrazono-1-methoxycarbonylmethylimidazolidin-4-one | HCID 136040605 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-Benzylidenehydrazono-3-ethoxycarbonylmethyl-1-methoxycarbonylmethylimidazolidin-4-one | HCID 54120721 | 44.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05422360 |
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| 出典データセット | uspto-grants-1995_06 |
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| ORD ID | ord-95f5bb33bf7440c88b09193ba4fb2a51 |
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| 出典メモ | uspto-grants-1995_06 |
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