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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736522Generated: October 26, 2026

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

https://huagongshe.com/reaction/1736522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl-4-phenyl-3-furoateHCID 15037153—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(4-Phenylfuran-3-yl)methanolHCID 15037154—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541221
Source datasetuspto-grants-1996_07
ORD IDord-2c8172e3ee4545e2bd8998bc43311047
Source noteuspto-grants-1996_07