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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326363Generated: October 26, 2026

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

https://huagongshe.com/reaction/326363

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 numberUS05268387
Source datasetuspto-grants-1993_12
ORD IDord-11b0d8f9251c4e85b8c0920957e4d9e3
Source noteuspto-grants-1993_12