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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23712Erstellt: 24. Oktober 2026

3-Pyridinecarboxaldehyde → 3-(Oxiran-2-yl)pyridine

https://huagongshe.com/de/reaction/23712

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-PyridinecarboxaldehydeHCID 10371—
EduktSodium HydroxideHCID 14798—
EduktTrimethylsulfonium methyl sulfateHCID 2760871—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(Oxiran-2-yl)pyridineHCID 1331956128,6%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 2.59 g of 3-pyridinecarboxaldehyde and 62 mg of tetra-n-butylammonium bromide in 60 mL CH2Cl2 at room temperature is added a solution of 10.0 g of trimethylsulfonium methylsulfate in 15 mL H2O. The resulting solution is set stirring and cooled to 0° C. Aqueous NaOH (50% w/w; 40 mL) is added in portions while stirring and the mixture subsequently refluxed for 1 h. After cooling to room temperature, the mixture is filtered and the filtrate extracted with CH2Cl2. The combined extracts are dried over MgSO4, filtered, and concentrated to yield a red oil, which is subjected to Kugelrohr distillation under high vacuum at 150° C. to yield 838 mg of the title compound as a clear, light yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06852731B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-80408188b07545bfbcf381ecf1bc3f7b
Quellennotizuspto-grants-2005_02