HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzaldehyde → HCID 118549294, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzaldehyde | HCID 240 | — |
| Edukt | Quinoline | HCID 7047 | — |
| Edukt | 18-Crown-6 | HCID 28557 | — |
| Edukt | Potassium Fluoride | HCID 522689 | — |
| Edukt | 2-(Trimethylsilyl)phenyl trifluoromethanesulfonate | HCID 3384007 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 118549294 | HCID 118549294 | 82% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09206196B1 |
| Quelldatensatz | uspto-grants-2015_12 |
| ORD ID | ord-d5582f5530874686956cf0c0555f154e |
| Quellennotiz | uspto-grants-2015_12 |