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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1090923Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/1090923

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 1.6 m 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 degrees and 3-phenyl-4-furaldehyde (Compound 18, 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
PatentnummerUS05082954
Quelldatensatzuspto-grants-1992_01
ORD IDord-daa206959471416aa1bca7fa73c966f7
Quellennotizuspto-grants-1992_01