HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 5,6-Dihydro-benzo[f]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tricyclohexylphosphonium Tetrafluoroborate | HCID 11710396 | — |
| Reactant | 3-Bromo-2-phenethyl-pyridine | HCID 58294397 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 5,6-Dihydro-benzo[f]quinoline | HCID 15873184 | — |
Reaction Steps
N,N-Dimethylacetamide (15 mL) is added to a flask charged with a stir bar, 3-bromo-2-phenethyl-pyridine (3.34 g), freshly dried K2CO3 (3.52 g), palladium(II) acetate (0.14 g), and tricyclohexylphosphonium tetrafluoroborate (0.47 g) and kept under argon atmosphere at room temperature. The flask is put into a 150° C. hot oil bath and the mixture is stirred therein for 2 h. After cooling the mixture to room temperature, the solvent is evaporated and the residue is chromatographed twice on silica gel (1. dichloromethane/methanol 98:2; 2. cyclohexane/ethyl acetate 90:10→50:50) to afford the title compound as an oil. Yield: 1.51 g (65% of theory); LC (method 1): tR=1.83 min; Mass spectrum (ESI+): m/z=182 [m+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09328072B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-6c85c3f435c94d85b5a77a43e4e446dc |
| Source note | uspto-grants-2016_05 |