Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 358779생성일: 2026년 10월 25일
Water → Methyl 4-(4-methoxycinnamoyl)-1(3,4,5-trimethoxybenzoyl)piperazine-2-carboxylate
https://huagongshe.com/reaction/358779
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Methyl 1-(3,4,5-trimethoxybenzoyl)piperazine-2-carboxylate | HCID 20066654 | — |
| 반응물 | 4-Methoxycinnamic acid chloride | HCID 53401772 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Methyl 4-(4-methoxycinnamoyl)-1(3,4,5-trimethoxybenzoyl)piperazine-2-carboxylate | HCID 53878437 | 78.9% |
반응 단계
A solution of 4-methoxy cinnamoyl chloride (0.3 g) in dichloromethane (4 ml) is added dropwise, taking 3 minutes at 0 ° C while stirring, to a mixture of methyl 1-(3,4,5-trimethoxybenzoyl)piperazine-2-carboxylate (0.57 g), triethylamine (0.4 g) and dichloromethane (12 ml). The reaction mixture is stirred for 30 minutes at room temperature, and then poured into water, followed by extraction with dichloromethane. The organic layer is washed with dilute hydrochloric acid, an aqueous solution of sodium hydrogencarbonate and water, successively, then the solvent is distilled off. The residue is purified by means of a silica gel column chromatography to give methyl 4-(4-methoxycinnamoyl)-1(3,4,5-trimethoxybenzoyl)piperazine-2-carboxylate (0.6 g) as a colorless oily product. This product is processed with ethyl ether to give colorless powder
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04997836 |
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| 출처 데이터셋 | uspto-grants-1991_03 |
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| ORD ID | ord-c6b2a9131e5340c2968dee10804eb67d |
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| 출처 메모 | uspto-grants-1991_03 |
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