Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2075192Erstellt: 25. Oktober 2026

Triethylamine → Benzofuran-5-yl(phenyl)methanone

https://huagongshe.com/reaction/2075192

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktDimethylsulfoxide-dichloromethaneHCID 21912085—
EduktBenzofuran-5-yl(phenyl)methanolHCID 58415371—
LösungsmittelDimethyl SulfoxideHCID 679—
ProduktBenzofuran-5-yl(phenyl)methanoneHCID 58415352—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of benzofuran-5-yl(phenyl)methanol (4.0 g, 18 mmol) and triethylamine (7.3 mL, 54 mmol) in 30 mL 1:1 DCM/DMSO under nitrogen at 0° C. was added a solution of SO3*py (8.5 g, 54 mmol) in 20 mL DMSO dropwise via addition funnel. The reaction was allowed to stir 5 h at 0° C. and was quenched by addition of water and 250 mL Et2O. The organic layer was washed with water, 1N HCl, 1N NaOH, brine, and was dried over sodium sulfate, filtered, and concentrated. The resulting solid benzofuran-5-yl(phenyl)methanone was used without further purification. MS (ESI) m/z: Calculated: 222.1; Observed: 223.0 (M++1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07919519B2
Quelldatensatzuspto-grants-2011_04
ORD IDord-770de3bda5be496e98d3f55f52d5696b
Quellennotizuspto-grants-2011_04