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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

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물Methyl 1-(3,4,5-trimethoxybenzoyl)piperazine-2-carboxylateHCID 20066654—
반응물4-Methoxycinnamic acid chlorideHCID 53401772—
용매DichloromethaneHCID 6344—
생성물Methyl 4-(4-methoxycinnamoyl)-1(3,4,5-trimethoxybenzoyl)piperazine-2-carboxylateHCID 5387843778.9%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04997836
출처 데이터셋uspto-grants-1991_03
ORD IDord-c6b2a9131e5340c2968dee10804eb67d
출처 메모uspto-grants-1991_03