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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488230Generated: October 30, 2026

3-Furancarboxaldehyde, 5-(triethylsilyl)- → HCID 11830655, compound

https://huagongshe.com/reaction/488230

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Furancarboxaldehyde, 5-(triethylsilyl)-HCID 10878438—
ReactantButyllithiumHCID 178418339—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 11830655HCID 11830655—

Reaction Conditions

Temperature0 °C

Reaction Steps

n-Butyl lithium (a 2.5 M solution in hexane; 4.4 ml, 11.0 mmol) was added dropwise to a suspension of methyltriphenylphosphonium bromide (3.93 g, 11 mmol) in THF (40ml) at 0 degrees C. under argon. After 2 hours stirring at 0 degrees C., a solution of 2-triethylsilyl-4-furaldehyde (1.54 g, 7.33 mmol) in THF (2 ml) was added. Stirring was continued at room temperature for 14 hours and the mixture was quenched with methanol/water 40 ml (1:1). Extraction (pentane) and evaporation of the dried (magnesium sulfate) extracts gave a residue, which was purified by flash chromatography on silica using pentane to give the titled furan. Rf (pentane) 0.75.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298633
Source datasetuspto-grants-1994_03
ORD IDord-ea9c3d33aa89439487fe9813971e5d96
Source noteuspto-grants-1994_03