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HRID 273955作成日:2026年10月27日

Ethyl-4-phenyl-3-furoate → (4-Phenylfuran-3-yl)methanol

https://huagongshe.com/reaction/273955

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl-4-phenyl-3-furoateHCID 15037153—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒TetrahydrofuranHCID 8028—
生成物(4-Phenylfuran-3-yl)methanolHCID 15037154—

反応手順

LiAlH4 (1.0M solution in hexane 1.14 ml, 1.14 mmol) was added dropwise to a solution of ethyl-4-phenyl-3-furoate (246 mg, assumed 1.28 mmol) in tetrahydrofuran (20 ml) at 0 degrees under argon. The solution was stirred and was allowed to warm to room temperature gradually over 1/2 hour. The mixture was quenched with saturated ammonium chloride and the organics were extracted into ethyl ether, and washed with H2O. Evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by flash chromatography on silica using 20% ethyl acetate/hexanes. This was further purified by recrystallation (hexane/ethyl ether) to give the title compound as pale yellow crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05387606
出典データセットuspto-grants-1995_02
ORD IDord-386df605fef84582903cae20aafa0cfd
出典メモuspto-grants-1995_02