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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273963Generated: October 25, 2026

3-Phenyl-2-triethylsilyl-4furaldehyde → 3-Phenyl-2-triethylsilyl-4-furanmethanol

https://huagongshe.com/reaction/273963

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Phenyl-2-triethylsilyl-4furaldehydeHCID 15037149—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product3-Phenyl-2-triethylsilyl-4-furanmethanolHCID 15037150—

Reaction Steps

LiAlH4 (1.0M solution in hexane, 1.48 ml, 1.48 mmol) was added dropwise to a solution of 3-phenyl-2-triethylsilyl-4-furaldehyde (422 mg, 1.48 mmol) in tetrahydrofuran (10 ml) at 0 degrees under argon. This mixture was warmed to room temperature, quenched with ice-cold 5% (V/V) hydrochloric acid and the organics were extracted into ethyl ether. The combined fractions were washed with saturated sodium bicarbonate, H2O and brine. The dried extracts (magnesium sulfate) were concentrated to an oil which was purified by flash chromatography on silica using 20% ethyl acetate/hexanes to give the title compound. IR (neat): 3300 (broad); 2953 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387606
Source datasetuspto-grants-1995_02
ORD IDord-967822ffd5dd4100847391fbab454d57
Source noteuspto-grants-1995_02