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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1501293Erstellt: 26. Oktober 2026

Benzaldehyde → HCID 118549294, Verbindung

https://huagongshe.com/reaction/1501293

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktQuinolineHCID 7047—
Edukt18-Crown-6HCID 28557—
EduktPotassium FluorideHCID 522689—
Edukt2-(Trimethylsilyl)phenyl trifluoromethanesulfonateHCID 3384007—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 118549294HCID 11854929482%

Reaktionsschritte

Following the general procedure, treatment of quinoline (0.064 g, 59 μL, 0.50 mmol) and benzaldehyde (0.080 g, 80 μL, 0.75 mmol) with 2-(trimethylsilyl)phenyl trifluoromethanesulfonate (0.179 g, 146 μL, 0.60 mmol) in the presence of KF (0.070 g, 1.2 mmol) and 18-crown-6 (0.317 g, 1.2 mmol) in THF (2.0 mL) at −10° C. to room temperature for 12 hrs followed by flash column chromatography (Pet. ether/EtOAc=75/25) of the crude reaction mixture afforded 5-phenyl-5H,6aH-benzo[4,5][1,3]oxazino[3,2-a]quinoline as a yellow solid (0.128 g, 82% yield, dr determined by 1H NMR analysis of crude reaction mixture is >20:1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09206196B1
Quelldatensatzuspto-grants-2015_12
ORD IDord-d5582f5530874686956cf0c0555f154e
Quellennotizuspto-grants-2015_12