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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 234791생성일: 2026년 10월 25일

[6-Methoxy-2-(4-methoxyphenyl)benzo[b]furan-3-yl][4-methoxyphenyl]methanol → [6-Methoxy-2-(4-methoxyphenyl)benzo[b]furan-3-yl][4-methoxyphenyl]methane

https://huagongshe.com/reaction/234791

반응식

참여 물질

역할이름HCID투입량
반응물[6-Methoxy-2-(4-methoxyphenyl)benzo[b]furan-3-yl][4-methoxyphenyl]methanolHCID 18925541—
반응물Aluminium lithium hydrideHCID 21226445—
용매PropylbenzeneHCID 7668—
생성물[6-Methoxy-2-(4-methoxyphenyl)benzo[b]furan-3-yl][4-methoxyphenyl]methaneHCID 18925542—

반응 단계

A solution of 400 mg (1.02 mmol) of [6-Methoxy-2-(4-methoxyphenyl)benzo[b]furan-3-yl][4-methoxyphenyl]methanol was dissolved in 10 mL of n-propylbenzene and 200 mg (5.25 mmol) of LiAlH4 was added. The reaction mixture was heated to reflux under a nitrogen atmoshere for 45 minutes. After sixteen hours, the reaction was quenched by the addition of 5 mL of water. To this suspension was added 3 mL of 15% (W/N) NaOH and an additional 3 mL of water. This suspension was filtered. The resulting filterate separated into two layers. The top (organic) layer was removed and evaporated to dryness. The crude product was chromatographed on silica eluted with 20% EtOAc in hexane. The final product was crystallized from ether. This yielded 100 mg of the title compound as a solid with a low melting point.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05596106
출처 데이터셋uspto-grants-1997_01
ORD IDord-1ac47aafe99a43dc9e239f504839bdfe
출처 메모uspto-grants-1997_01