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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 52007Erstellt: 23. Oktober 2026

Dimedone → 5-(4,6-Dimethoxypyrimidin-2-yl)oxy-3-ethylthiocarbonyl-2-methylbenzofuran-4-carboxylic Acid

https://huagongshe.com/de/reaction/52007

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimedoneHCID 31358—
EduktAllyl 5-(4,6-dimethoxypyrimidin-2-yl)oxy-3-ethylthiocarbonyl-2-methylbenzofuran-4-carboxylateHCID 53832981—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-(4,6-Dimethoxypyrimidin-2-yl)oxy-3-ethylthiocarbonyl-2-methylbenzofuran-4-carboxylic AcidHCID 5446801991,4%

Reaktionsschritte

1.60 g of allyl 5-(4,6-dimethoxypyrimidin-2-yl)oxy-3-ethylthiocarbonyl-2-methylbenzofuran-4-carboxylate and 0.54 g of dimedone were dissolved in 14 ml of tetrahydrofuran, and 40 mg of tetrakistriphenylphosphine palladium (0) was added thereto under a nitrogen atmosphere. The mixture was stirred at room temperature for 3 hours. The reaction solution was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=2/1) to obtain 1.33 g (yield: 91%) of the desired compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05616537
Quelldatensatzuspto-grants-1997_04
ORD IDord-20301908661145a2bcc9f8c17eecf4a7
Quellennotizuspto-grants-1997_04