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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1057Erstellt: 23. Oktober 2026

(E)-ethyl 3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]acrylate → 3-[6-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]propanol

https://huagongshe.com/de/reaction/1057

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(E)-ethyl 3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]acrylateHCID 19694380—
KatalysatorHCID 178418390HCID 178418390—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-[6-(5-Methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]propanolHCID 19694387—

Reaktionsschritte

To a solution of (E)-ethyl 3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]acrylate (1.30 g) in tetrahydrofuran (50 ml), palladium-carbon (5%, 0.70 g) was added, followed by catalytic reduction at room temperature and under an atmospheric pressure of 1 atm. After the catalyst was filtered off, sodium borohydride (0.61 g) was added to the filtrate, followed by dropwise addition of methanol (10 ml) under refluxing conditions. After heating under refluxing conditions for 1 hour, the reaction mixture was poured over water and neutralized with 2N hydrochloric acid, followed by extraction with ethyl acetate. After the ethyl acetate layer was washed with water and dried (MgSO4), the solvent was distilled off; the residue was subjected to silica gel column chromatography. From the fraction eluted with ethyl acetate-chloroform (1:5, v/v), 3-[6-(5-methyl-2-phenyl-4-oxazolylmethoxy)-2-benzofuranyl]propanol was obtained as an oily substance (0.90 g, 77%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723479
Quelldatensatzuspto-grants-1998_03
ORD IDord-9fb75830acba4d7b95932f5349ef385f
Quellennotizuspto-grants-1998_03