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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

반응식

참여 물질

역할이름HCID투입량
반응물(E)-ethyl 3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]acrylateHCID 19694380—
촉매HCID 178418390HCID 178418390—
용매TetrahydrofuranHCID 8028—
생성물3-[6-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]propanolHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723479
출처 데이터셋uspto-grants-1998_03
ORD IDord-9fb75830acba4d7b95932f5349ef385f
출처 메모uspto-grants-1998_03