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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1017002Erstellt: 24. Oktober 2026

Toluene → 3-(Furan-3-yl)benzaldehyde

https://huagongshe.com/de/reaction/1017002

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
PatentnummerUS06476057B1
Quelldatensatzuspto-grants-2002_11
ORD IDord-0e96dedeb2db434abd0ebaa704af1346
Quellennotizuspto-grants-2002_11