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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Vanillin | HCID 1183 | — |
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | HCID 22563405 | HCID 22563405 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 3-Methoxy-4-[(2-piperidin-1-yl-1,3-thiazol-4-yl)methoxy]benzaldehyde | HCID 85954618 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07368578B2 |
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| Quelldatensatz | uspto-grants-2008_05 |
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| ORD ID | ord-389c11ecbdc64047904d6beaa730a9b8 |
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| Quellennotiz | uspto-grants-2008_05 |
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