Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1740915생성일: 2026년 10월 26일
(Z)-2-[3-[4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]phenyl]-2-propenyl]-1,3-dioxane → 2-[3-[4-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]phenyl]propyl]-1,3-dioxane
https://huagongshe.com/reaction/1740915
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | (Z)-2-[3-[4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]phenyl]-2-propenyl]-1,3-dioxane | HCID 11811571 | — |
| 촉매 | HCID 178418390 | HCID 178418390 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 2-[3-[4-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy]phenyl]propyl]-1,3-dioxane | HCID 11025902 | 96% |
반응 단계
A mixture of (Z)-2-[3-[4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]phenyl]-2-propenyl]-1,3-dioxane (5.0 g), palladium-carbon (5%, 0.1 g) and ethanol (100 ml) was subjected to catalytic hydrogenation at room temperature under one 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 hexane-ethyl acetate (1:1), 2-[3-[4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]phenyl]propyl]-1,3-dioxane (4.8 g, 96%) was obtained. NMR (δ ppm in CDCl3): 1.25-1.4(1H,m), 1.5-1.8(4H,m), 1.9-2.2(1H,m), 2.37(3H,s), 2.54(2H,t,J=7 Hz), 2.96(2H,t,J=6.5 Hz), 3.65-3.85(2H,m), 4.0-4.15(2H,m), 4.21(2H,t,J=6.5 Hz), 4.50(1H,t,J=5 Hz), 6.80(2H,d,J=9 Hz), 7.06(2H,d,J=9 Hz), 7.35-7.5(3H,m), 7.9-8.0(2H,m).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05972970 |
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| 출처 데이터셋 | uspto-grants-1999_10 |
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| ORD ID | ord-1cd8adfbaf8a41beb827099e40da967a |
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| 출처 메모 | uspto-grants-1999_10 |
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