Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1031507생성일: 2026년 10월 27일
1,2-Dimethoxyethane → 4-[3-(5-(4-Chlorophenoxy)-2-pyridyl)-3-(3,4-dimethoxyphenyl)acryloxy]morpholine
https://huagongshe.com/reaction/1031507
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 반응물 | Phosphonic acid, [2-(4-morpholinyl)-2-oxoethyl]-, diethyl ester | HCID 11207805 | — |
| 반응물 | 5-(4-Chlorophenoxy)-2-(3,4-dimethoxybenzoyl)pyridine | HCID 14823233 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 반응물 | HCID 178418922 | HCID 178418922 | — |
| 생성물 | 4-[3-(5-(4-Chlorophenoxy)-2-pyridyl)-3-(3,4-dimethoxyphenyl)acryloxy]morpholine | HCID 54517826 | — |
반응 단계
In 1,2-dimethoxyethane (10 ml) was dissolved diethylphosphonoacetic acid morpholide (210 mg), to which was added 90% potassium tert-butoxide (100 mg). To the mixture was added, after the tert-butoxy potassium was completely dissolved, 5-(4-chlorophenoxy)-2-(3,4-dimethoxybenzoyl)pyridine (240 mg). The mixture was stirred for one hour at room temperature and for 6 hours at 50° C. to 60° C. The reaction mixture was concentrated, and there was added water (30 ml), followed by extraction with ethyl acetate (70 ml×2). The extract solution was dried over anhydrous magnesium sulfate, and was subjected to filtration to remove the magnesium sulfate. The filtrate was concentrated and purified by means of a silica gel column chromatography (eluted with ethyl acetate) to obtain 4-[3-(5-(4-chlorophenoxy)-2-pyridyl)-3-(3,4-dimethoxyphenyl)acryloxy]morpholine (Compound No.88) (300 mg) as a resinous solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04954497 |
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| 출처 데이터셋 | uspto-grants-1990_09 |
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| ORD ID | ord-1289fb28f3824ab5b155337c9044b748 |
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| 출처 메모 | uspto-grants-1990_09 |
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