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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1049생성일: 2026년 10월 23일

5-[6-(5-Methyl-2-phenyl-4-oxazolyl-methoxy)-2-benzofuranylmethylidene]-2,4-thiazolidinedione → 5-[6-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranylmethyl]-2,4-thiazolidinedione

https://huagongshe.com/ko/reaction/1049

반응식

참여 물질

역할이름HCID투입량
반응물5-[6-(5-Methyl-2-phenyl-4-oxazolyl-methoxy)-2-benzofuranylmethylidene]-2,4-thiazolidinedioneHCID 85452177—
촉매HCID 178418390HCID 178418390—
용매TetrahydrofuranHCID 8028—
생성물5-[6-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranylmethyl]-2,4-thiazolidinedioneHCID 8675217138%

반응 단계

A mixture of 5-[6-(5-methyl-2-phenyl-4-oxazolyl-methoxy)-2-benzofuranylmethylidene]-2,4-thiazolidinedione (0.80 g), palladium-carbon (5%, 1.60 g) and tetrahydrofuran (250 ml) was subjected to catalytic reduction at room temperature under a hydrogen pressure of 3.2 kgf/cm2 for 8 hours. After the catalyst was filtered off, the filtrate was subjected to catalytic reduction under constant conditions for additional 16 hours. After the catalyst was filtered off, the filtrate was concentrated under reduced pressure; the residue was subjected to silica gel column chromatography. From the fraction eluted with ethyl acetate-chloroform (1:5, v/v), crystals of 5-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranylmethyl]-2,4-thiazolidinedione (0.305 g, 38%) were obtained, which was then recrystallized from dichloromethane-methanol to yield yellow needles having a melting point of 179° to 180° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723479
출처 데이터셋uspto-grants-1998_03
ORD IDord-f01dc9a32ad94d4099a32d40a2b8c964
출처 메모uspto-grants-1998_03