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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1058Erstellt: 24. Oktober 2026

(E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]propen-1-ol → (E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]acrolein

https://huagongshe.com/de/reaction/1058

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]propen-1-olHCID 19694368—
KatalysatorHCID 178418406HCID 178418406—
LösungsmittelDichloromethaneHCID 6344—
Produkt(E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]acroleinHCID 1969437889%

Reaktionsschritte

A mixture of (E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]propen-1-ol (3.85 g), activated manganese dioxide (8.00 g) and dichloromethane (150 ml ) was stirred at room temperature for 2 hours. After the insoluble portion was filtered off, the filtrate was concentrated to yield crystals of (E)-3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]acrolein (3.40 g, 89%), which was then recrystallized from dichloromethane-isopropyl ether to yield colorless prisms having a melting point of 132° to 133° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723479
Quelldatensatzuspto-grants-1998_03
ORD IDord-20c9273eacd748b48025e08d9d4eba7a
Quellennotizuspto-grants-1998_03