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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 273962Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/273962

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorotriethylsilaneHCID 13819—
Edukt1-MethylpiperazineHCID 53167—
Edukt4-Phenyl-3-furaldehydeHCID 15037148—
EduktButyllithiumHCID 178418339—
EduktCID 53628100HCID 178418400—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
LösungsmittelCyclohexaneHCID 8078—
Produkt3-Phenyl-2-triethylsilyl-4furaldehydeHCID 15037149—

Reaktionsschritte

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 11/2 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05387606
Quelldatensatzuspto-grants-1995_02
ORD IDord-10d73349a7664917a2998a5e8a0a4ab0
Quellennotizuspto-grants-1995_02