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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50482Erstellt: 24. Oktober 2026

Toluene → 3-(Furan-3-yl)benzaldehyde

https://huagongshe.com/de/reaction/50482

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

EX-601A) 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
PatentnummerUS06710089B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-d62f8cb5cdc0409eab9dad90164d7a31
Quellennotizuspto-grants-2004_03