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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 326366Erstellt: 23. Oktober 2026

Methyl iodide → 2-Methyl-4-phenyl-3-furaldehyde

https://huagongshe.com/de/reaction/326366

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
Edukt1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
Edukt4-Phenyl-3-furaldehydeHCID 15037148—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produkt2-Methyl-4-phenyl-3-furaldehydeHCID 15037159—

Reaktionsschritte

n-Butyllithium (a 1.6m solution in hexane, 2.43 ml, 3.89 mmol) was added to a solution of trimethylethylenediamine (397 mg, 3.89 mmol) in tetrahydrofuran (25 ml) at 0 degrees under argon. After 20 minutes the solution was cooled to -78 degres and 4-phenyl-3-furaldehyde (608 mg, 3.35 mmol) was added. This mixture was allowed to gradually warm to -20 degrees and stirred for 11/2 hours, then recooled to -78 degrees before n-butyllithium (a 1.6M solution in hexane, 2.43 ml, 3.89 mmol) was added dropwise. The stirring mixture was again gradually warmed to -20 degrees and stirred for 2 hours before iodomethane (2.56 g 17.67 mmol) was added. After stirring for 18 hours at -20 degrees the reaction was quenched with ice-cold 10% (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 20% ethyl ether/hexanes to give the title aldehyde.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05268387
Quelldatensatzuspto-grants-1993_12
ORD IDord-4905bc23f6ca4ea7b240873898cccace
Quellennotizuspto-grants-1993_12