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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271981Generated: October 28, 2026

2-Tetralone → 5,6-Dihydro-benzo[f]quinoline

https://huagongshe.com/reaction/2271981

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-TetraloneHCID 68266—
ReactantPropargylamineHCID 239041—
SolventEthanolHCID 702—
Product5,6-Dihydro-benzo[f]quinolineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120769B2
Source datasetuspto-grants-2015_09
ORD IDord-2038b71dfe734d9986784ead32bdf204
Source noteuspto-grants-2015_09