Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1016999Erstellt: 25. Oktober 2026

1,4-Dioxane → Ketone, 3-furyl phenyl

https://huagongshe.com/reaction/1016999

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-DioxaneHCID 31275—
Edukt3-BromobenzaldehydeHCID 76583—
EduktPotassium FluorideHCID 522689—
Edukt2-(Tributylstannyl)furanHCID 4393688—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelEthyl AcetateHCID 8857—
ProduktKetone, 3-furyl phenylHCID 20164086%

Reaktionsschritte

EX-592A) To a dioxane (20 mL) solution of 3-bromobenzaldehyde (0.63 mL, 5.4 mmol) was added 2-(tributylstannyl)furan (1.89 mL, 6.00 mL) and Pd(PPh3)2Cl2 (0.21 g, 0.30 mmol). The mixture was heated to reflux under argon for 1.5 h. The cooled mixture was poured into a mixture of saturated KF and ethyl acetate and stirred 18 h. The slurry was filtered through celite. The organic layer was separated, 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 0.80 g (86%) of the desired 3-(2-furanyl)benzaldehyde product as an yellow oil which solidified upon standing. MS: m/z=173.1 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06476057B1
Quelldatensatzuspto-grants-2002_11
ORD IDord-ea143187af884b6db95116ee8fce25d4
Quellennotizuspto-grants-2002_11