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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 363521Erstellt: 25. Oktober 2026

Sodium Carbonate → [2,2'-Bithiophene]-5-carboxaldehyde

https://huagongshe.com/reaction/363521

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt1,4-DioxaneHCID 31275—
Edukt5-Formyl-2-thiophenecarboxylic AcidHCID 818882—
Edukt2-Thiopheneboronic acidHCID 2733960—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
Produkt[2,2'-Bithiophene]-5-carboxaldehydeHCID 364428—

Reaktionsschritte

To a solution of thien-2-ylboronic acid (0.939 g, 7.34 mmol) and Na2CO3 (2.40 g, 22.6 mmol) in water (75 mL) is added p-dioxane (75 mL). This mixture is treated sequentially with 5-carboxy-2-thiophenecarboxaldehyde (1.43 g, 7.48 mmol) and palladium (II) acetate (151 mg, 0.673 mmol) and allowed to stir at ambient temperature for 16 hours. The solvent is evaporated in vacuo. To the residue is added EtOAc (400 mL) and water (300 mL). The aqueous layer is acidified to pH 1 with 1.0N aq. HCl. The aqueous layer is extracted with EtOAc (2×200 mL). The organic extracts are combined, washing with brine (200 mL), 5% aq. Na2S2O3 (200 mL), sat. aq. NaCl (200 mL), drying (Na2SO4), and the solvent evaporation in vacuo affords the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05874452
Quelldatensatzuspto-grants-1999_02
ORD IDord-e97527c8980b4262893c7b5db2e97ea9
Quellennotizuspto-grants-1999_02