HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Tetralone → 5,6-Dihydro-benzo[f]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Tetralone | HCID 68266 | — |
| Reactant | Propargylamine | HCID 239041 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5,6-Dihydro-benzo[f]quinoline | HCID 15873184 | — |
Reaction Steps
Propargylamine (5 mL) is added to a flask charged with a stir bar, 2-tetralone (10.00 g), NaAuCl4*2H2O (0.65 g), and ethanol (50 mL) (caution: a very exothermic reaction may evolve afterwards→keep an ice bath at hand). The resulting mixture is stirred at room temperature for 15 min and then at reflux temperature for 1 h. After cooling the mixture to room temperature, the solvent is evaporated and the residue is chromatographed on silica gel (cyclohexane/ethyl acetate 60:40) to afford the title compound as an oil. Yield: 6.78 g (56% of theory); LC (method 1): tR=1.81 min; Mass spectrum (ESI+): m/z=182 [M+H]+. Alternatively, the reaction may be conducted in a microwave oven heating with microwave irradiation to 100° C. for 10 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120769B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-2038b71dfe734d9986784ead32bdf204 |
| Source note | uspto-grants-2015_09 |