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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2221551Erstellt: 26. Oktober 2026

Vanillin → 3-Methoxy-4-[(2-piperidin-1-yl-1,3-thiazol-4-yl)methoxy]benzaldehyde

https://huagongshe.com/reaction/2221551

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktVanillinHCID 1183—
EduktDimethylformamideHCID 6228—
EduktPotassium CarbonateHCID 11430—
EduktHCID 22563405HCID 22563405—
LösungsmittelWaterHCID 962—
Produkt3-Methoxy-4-[(2-piperidin-1-yl-1,3-thiazol-4-yl)methoxy]benzaldehydeHCID 8595461888%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 1-(4-chloromethyl-1,3-thiazol-2-yl)piperidine (1.00 g), potassium carbonate (0.64 g), vanillin (0.70 g) and N,N-dimethylformamide (30 mL) was stirred at 80° C. for 2 hrs. Water was poured into the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give 3-methoxy-4-[(2-piperidin-1-yl-1,3-thiazol-4-yl)methoxy]benzaldehyde as colorless crystals (1.34 g, 88%) from a fraction eluted with ethyl acetate-hexane (1:1, v/v). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 129-130° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07368578B2
Quelldatensatzuspto-grants-2008_05
ORD IDord-389c11ecbdc64047904d6beaa730a9b8
Quellennotizuspto-grants-2008_05