Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1057생성일: 2026년 10월 25일
(E)-ethyl 3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]acrylate → 3-[6-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]propanol
https://huagongshe.com/reaction/1057
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | (E)-ethyl 3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]acrylate | HCID 19694380 | — |
| 촉매 | HCID 178418390 | HCID 178418390 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-[6-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]propanol | HCID 19694387 | — |
반응 단계
To a solution of (E)-ethyl 3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]acrylate (1.30 g) in tetrahydrofuran (50 ml), palladium-carbon (5%, 0.70 g) was added, followed by catalytic reduction at room temperature and under an atmospheric pressure of 1 atm. After the catalyst was filtered off, sodium borohydride (0.61 g) was added to the filtrate, followed by dropwise addition of methanol (10 ml) under refluxing conditions. After heating under refluxing conditions for 1 hour, the reaction mixture was poured over water and neutralized with 2N hydrochloric acid, followed by extraction with ethyl acetate. After the ethyl acetate layer was washed with water and dried (MgSO4), the solvent was distilled off; the residue was subjected to silica gel column chromatography. From the fraction eluted with ethyl acetate-chloroform (1:5, v/v), 3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]propanol was obtained as an oily substance (0.90 g, 77%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05723479 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-9fb75830acba4d7b95932f5349ef385f |
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| 출처 메모 | uspto-grants-1998_03 |
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