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HRID 234791作成日:2026年10月26日

[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

反応式

関与物質

役割名称HCID仕込み量
反応物[6-Methoxy-2-(4-methoxyphenyl)benzo[b]furan-3-yl][4-methoxyphenyl]methanolHCID 18925541—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒PropylbenzeneHCID 7668—
生成物[6-Methoxy-2-(4-methoxyphenyl)benzo[b]furan-3-yl][4-methoxyphenyl]methaneHCID 18925542—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05596106
出典データセットuspto-grants-1997_01
ORD IDord-1ac47aafe99a43dc9e239f504839bdfe
出典メモuspto-grants-1997_01