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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 990525Erstellt: 27. Oktober 2026

Toluene → 3-(Furan-3-yl)benzaldehyde

https://huagongshe.com/reaction/990525

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktPotassium CarbonateHCID 11430—
Edukt3-BromofuranHCID 89164—
Edukt3-Formylphenylboronic acidHCID 2734356—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-(Furan-3-yl)benzaldehydeHCID 2350601010%

Reaktionsschritte

To a toluene (10 mL) solution of 3-bromofuran (0.54 mL, 6.0 mmol) was added 3-formylphenylboronic acid (1.00 g, 6.7 mmol) and DMF (4 mL). To the resulting solution was added K2CO3 (1.85 g, 13.4 mmol) and Pd(PPh3)4 (0.40 g, 0.35 mmol). The slurry was heated to reflux under argon for 2 h. The cooled mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4) and evaporated to an oil. Purification by flash chromatography on silica gel eluting with 5% ethyl acetate in hexane gave 0.10 g (10%) of the desired 3-(3-furanyl)benzaldehyde product as a yellow oil. MS: m/z=173.0 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06458852B1
Quelldatensatzuspto-grants-2002_10
ORD IDord-d331e814c22b41ca998605fc7d95bf70
Quellennotizuspto-grants-2002_10