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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

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DimethoxyethaneHCID 8071—
반응물Phosphonic acid, [2-(4-morpholinyl)-2-oxoethyl]-, diethyl esterHCID 11207805—
반응물5-(4-Chlorophenoxy)-2-(3,4-dimethoxybenzoyl)pyridineHCID 14823233—
반응물Potassium tert-butoxideHCID 23665647—
반응물HCID 178418922HCID 178418922—
생성물4-[3-(5-(4-Chlorophenoxy)-2-pyridyl)-3-(3,4-dimethoxyphenyl)acryloxy]morpholineHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04954497
출처 데이터셋uspto-grants-1990_09
ORD IDord-1289fb28f3824ab5b155337c9044b748
출처 메모uspto-grants-1990_09