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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736529Generated: November 3, 2026

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

https://huagongshe.com/reaction/1736529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotriethylsilaneHCID 13819—
Reactant1-MethylpiperazineHCID 53167—
Reactant4-Phenyl-3-furaldehydeHCID 15037148—
ReactantButyllithiumHCID 178418339—
ReactantCID 53628100HCID 178418400—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventCyclohexaneHCID 8078—
Product3-Phenyl-2-triethylsilyl-4furaldehydeHCID 15037149—

Reaction Steps

n-Butyllithium (a 1.42M solution in hexane, 2.33 ml, 3.31 mmol) was added to a solution of 1-methylpiperazine (331 mg. 3.31 mmol) in tetrahydrofuran (15 ml) at 0 degrees under argon. After 15 minutes the solution was cooled to -78 degrees and 4-phenyl-3-furaldehyde (517 mg, 3.01 mmol) was added. This mixture was warmed to 0 degrees and stirred for 15 minutes, then recooled to -78 degrees before sec-butyllithium (a 1.3M solution in cyclohexane, 2.77 ml, 3.61 mmol) was added dropwise. This solution was stirred 12 hours at -78 degrees C. before chlorotriethylsilane (1.81 g, 12.02 mmol) was added. The mixture was allowed to warm gradually to room temperature and stirred an additional 1 1/2 hours. The reaction was 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. Evaporation of the dried (magnesium sulfate) extracts gave an oil which was purified by flash chromatography on silica using 10% ethyl acetate/hexanes to give the title aldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541221
Source datasetuspto-grants-1996_07
ORD IDord-f81feaf571804237bae9066797b847bc
Source noteuspto-grants-1996_07