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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2120238Erstellt: 26. Oktober 2026

Sodium Carbonate → 4-Methoxy-3-(thiophen-2-yl)benzaldehyde

https://huagongshe.com/reaction/2120238

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt3-Bromo-4-methoxybenzaldehydeHCID 98662—
Edukt2-Thiopheneboronic acidHCID 2733960—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthanolHCID 702—
LösungsmittelTolueneHCID 1140—
Produkt4-Methoxy-3-(thiophen-2-yl)benzaldehydeHCID 2198102487%

Reaktionsschritte

Tetrakis(triphenylphosphine)palladium(0) (0.24 g, 0.21 mmol) was added to a solution of 4-methoxy-3-bromobenzaldehyde (1.5 g, 6.98 mmol) in toluene (15 mL) and ethanol (15 mL), followed by a 2 M aqueous solution of sodium carbonate (14 mL, 28 mmol). To this mixture was added thiophene-2-boronic acid (0.98 g, 7.68 mmol), and the mixture was heated to reflux. After 3 hours, the reaction was partitioned between water (100 mL) and ethyl acetate (250 mL). The organic layer was washed with saturated aqueous sodium bicarbonate (75 mL) and brine (75 mL), dried with magnesium sulfate and concentrated. Chromatography (silica, 20% ethyl acetate/hexanes) afforded 1.3 g (87%) of 4-methoxy-3-thiophen-2-yl-benzaldehyde as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06689806B1
Quelldatensatzuspto-grants-2004_02
ORD IDord-6f61e9f503924afaa8e686c132437d02
Quellennotizuspto-grants-2004_02