Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 734188Erstellt: 25. Oktober 2026

7,8-Dihydroxyflavone → HCID 59052279, Verbindung

https://huagongshe.com/reaction/734188

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt7,8-DihydroxyflavoneHCID 1880—
EduktAcetonitrileHCID 6342—
Edukt1-Butyne, 3-chloro-3-methyl-HCID 70679—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ProduktHCID 59052279HCID 5905227969%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a suspension of 7,8-dihydroxy-2-phenyl-chromen-4-one (510 mg, 2 mmol) and CuCl2 (16 mg, 0.12 mmol) in acetonitrile (3 mL) was added 3-chloro-3-methyl-1-butyne (0.5 mL, 4.56 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (0.78 mL, 5.2 mmol) slowly at 0° C. The dark mixture was stirred at 0° C. for 5 h and then at room temperature overnight. The solvent was evaporated and the residue was purified by column chromatography (SiO2, EtOAc:hexanes/10-50%) to give the title compound as a white solid (540 mg, 69%): 1H NMR (CDCl3, 300 MHz) δ 8.02 (m, 2H), 7.96 (d, J=9.0 Hz, 1H), 7.69 (d, J=9.0 Hz, 1H), 7.53 (m, 3H), 6.78 (s, 1H), 2.66 (s, 1H), 2.26 (s, 1H), 1.81 (s, 6H), 1.76 (s, 6H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07592143B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-9bcbb5461b234b19b6e606b26e50ecfb
Quellennotizuspto-grants-2009_09