HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1049Erstellt: 23. Oktober 2026
5-[6-(5-Methyl-2-phenyl-4-oxazolyl-methoxy)-2-benzofuranylmethylidene]-2,4-thiazolidinedione → 5-[6-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranylmethyl]-2,4-thiazolidinedione
https://huagongshe.com/de/reaction/1049
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 5-[6-(5-Methyl-2-phenyl-4-oxazolyl-methoxy)-2-benzofuranylmethylidene]-2,4-thiazolidinedione | HCID 85452177 | — |
| Katalysator | HCID 178418390 | HCID 178418390 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 5-[6-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranylmethyl]-2,4-thiazolidinedione | HCID 86752171 | 38% |
Reaktionsschritte
A mixture of 5-[6-(5-methyl-2-phenyl-4-oxazolyl-methoxy)-2-benzofuranylmethylidene]-2,4-thiazolidinedione (0.80 g), palladium-carbon (5%, 1.60 g) and tetrahydrofuran (250 ml) was subjected to catalytic reduction at room temperature under a hydrogen pressure of 3.2 kgf/cm2 for 8 hours. After the catalyst was filtered off, the filtrate was subjected to catalytic reduction under constant conditions for additional 16 hours. After the catalyst was filtered off, the filtrate was concentrated under reduced pressure; the residue was subjected to silica gel column chromatography. From the fraction eluted with ethyl acetate-chloroform (1:5, v/v), crystals of 5-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranylmethyl]-2,4-thiazolidinedione (0.305 g, 38%) were obtained, which was then recrystallized from dichloromethane-methanol to yield yellow needles having a melting point of 179° to 180° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05723479 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-f01dc9a32ad94d4099a32d40a2b8c964 |
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| Quellennotiz | uspto-grants-1998_03 |
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