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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1267303생성일: 2026년 10월 27일

5-[4-[2-[5-Methyl-2-(3-methylphenyl)-4-oxazolyl]ethoxy]cinnamylidene]-2,4-oxazolidinedione → 5-[3-[4-[2-[5-Methyl-2-(3-methylphenyl)-4-oxazolyl]ethoxy]phenyl]propyl]-2,4-oxazolidinedione

https://huagongshe.com/reaction/1267303

반응식

참여 물질

역할이름HCID투입량
반응물5-[4-[2-[5-Methyl-2-(3-methylphenyl)-4-oxazolyl]ethoxy]cinnamylidene]-2,4-oxazolidinedioneHCID 57037009—
촉매HCID 178418390HCID 178418390—
용매1,4-DioxaneHCID 31275—
생성물5-[3-[4-[2-[5-Methyl-2-(3-methylphenyl)-4-oxazolyl]ethoxy]phenyl]propyl]-2,4-oxazolidinedioneHCID 1587242996%

반응 단계

A mixture of 5-[4-[2-[5-methyl-2-(3-methylphenyl)-4-oxazolyl]ethoxy]cinnamylidene]-2,4-oxazolidinedione (0.29 g), palladium-carbon (10%, 0.1 g) and dioxane (50 ml) was subjected to catalytic hydrogenation at room temperature under atmospheric pressure. The catalyst was filtered off, and the filtrate was concentrated under reduced pressure. The concentrate was purified by means of a silica gel column chromatography. From the fractions eluted with chloroform-methanol (100:3) was obtained 5-[3-[4-[2-[5-methyl-2-(3-methylphenyl)-4-oxazolyl]ethoxy]phenyl]propyl]-2,4-oxazolidinedione (0.28 g, 96%). This product was recrystallized from dichloromethane-methanol to give colorless prisms, m.p.149-150° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06552058B1
출처 데이터셋uspto-grants-2003_04
ORD IDord-62785fad55c348eda698dd1cf279408e
출처 메모uspto-grants-2003_04