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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 446055Erstellt: 26. Oktober 2026

Water → 5-(3-Iodophenyl)furan-2-carbaldehyde

https://huagongshe.com/reaction/446055

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium CarbonateHCID 10340—
EduktBenzene, 1,3-diiodo-HCID 12270—
Edukt5-Formylfuran-2-boronic acidHCID 2734355—
KatalysatorHCID 178418397HCID 178418397—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt5-(3-Iodophenyl)furan-2-carbaldehydeHCID 4315582225,9%

Reaktionsschritte

5-Formyl-2-furanboronic acid (280 mg, 2 mmol) and 1,3-diiodobenzene (660 mg, 2 mmol) were dissolved in 1,2-dimethoxyethane (15 mL), tetrakis(triphenylphosphine)palladium (114 mg, 0.1 mmol) was added thereto, 2 mol/L sodium carbonate (4.6 mL) was then added thereto, and the mixture was heated to reflux for 3 hours while stirring. After the reaction was completed water (20 mL) was added, and extraction with ethyl acetate (20 mL×2) was carried out. The organic layer was washed with saturated brine, water was removed using anhydrous sodium sulfate, the solvent was then removed by evaporation under reduced pressure, and the residue was subjected to silica gel column chromatography using ethyl acetate/hexane (3/7 (volume ratio)) as an eluent, to give 5-(3-iodophenyl)furan-2-carbaldehyde in a yield of 155 mg (yield 25.9%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08476449B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-fba0408a89e94c6195eec18ef6c3a1bd
Quellennotizuspto-grants-2013_07