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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1860791Erstellt: 26. Oktober 2026

Water → 3-(4-Methoxy-3-thiophen-3-ylbenzylidene)-1,3-dihydroindol-2-one

https://huagongshe.com/reaction/1860791

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium CarbonateHCID 10340—
EduktThiophene-3-boronic acidHCID 581760—
Edukt3-(3-Bromo-4-methoxybenzylidene)-1,3-dihydroindol-2-oneHCID 2803107—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthanolHCID 702—
LösungsmittelTolueneHCID 1140—
Produkt3-(4-Methoxy-3-thiophen-3-ylbenzylidene)-1,3-dihydroindol-2-oneHCID 5370652050%

Reaktionsschritte

Tetrakis(triphenylphosphine)palladium(0) (0.02 g, 0.02 mmol) was added to a solution of 3-(3-bromo-4-methoxybenzylidene)-1,3-dihydroindol-2-one (0.2 g, 0.61 mmol) in toluene (1 ml) and ethanol (1 ml), followed by addition of 2M aqueous sodium carbonate (1.2 ml, 2.4 mmol). To this mixture was added thiophene-3-boronic acid (0.09 g, 0.67 mmol) and the mixture was held at 100° C. in a sealed tube for 12 hours. The reaction was then poured into water (50 ml) and extracted with ethyl acetate (2×100 ml). The combined organic layers were washed with saturated aqueous sodium bicarbonate (50 ml) and brine (50 ml), dried over magnesium sulfate and concentrated. Chromatography (silica, methylene chloride then 30-40% ethyl acetate/hexanes) afforded 0.1 g (50%) of 3-(4-methoxy-3-thiophen-3-ylbenzylidene)-1,3-dihydroindol-2-one as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06531502B1
Quelldatensatzuspto-grants-2003_03
ORD IDord-b187382ae0ef4d0fa4da8c4fffe5ef2d
Quellennotizuspto-grants-2003_03