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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033516Generated: November 1, 2026

Phenethylamine → 5,6,7,8-Tetrahydro-5-[(2-phenylethyl)amino]-1-(2-propenyl)-2(1H)-quinolinone

https://huagongshe.com/reaction/1033516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethylamineHCID 1001—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant5,6,7,8-tetrahydro-5-oxo-1-(2-propenyl)-2(1H)-quinolinoneHCID 10330512—
SolventTolueneHCID 1140—
Product5,6,7,8-Tetrahydro-5-[(2-phenylethyl)amino]-1-(2-propenyl)-2(1H)-quinolinoneHCID 1840911189.6%

Reaction Steps

A mixture of phenethylamine (6.1 g), 5,6,7,8-tetrahydro-5-oxo-1-(2-propenyl)-2(1H)-quinolinone (10.0 g), and a catalytic amount of para-toluenesulfonic acid was heated in refluxing toluene (150 ml), with azeotropic removal of water, for 18 hrs. The solution was cooled and washed with water. The aqueous phase was extracted with dichloromethane, and the combined organic layers were washed with brine, dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated. Sodium borohydride (1.8 g) was added to the residue in ethyl alcohol (150 ml) and the resulting mixture was stirred at room temperature for 0.5 hr. The mixture was concentrated in vacuo, and the residue was quenched with water. The mixture was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated. The residue was purified by high performance liquid chromatography (silica gel, eluted with methanol/ethyl acetate) to afford 13.6 g (89%) of product. Recrystallization from diethyl ether/petroleum ether provided the analytical sample, mp 60°-62° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05310914
Source datasetuspto-grants-1994_05
ORD IDord-35dadbd445964c61a5a1e852eb72be8b
Source noteuspto-grants-1994_05