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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195177Generated: November 2, 2026

3,4-Dichlorophenethylamine → HCID 10383281, compound

https://huagongshe.com/reaction/1195177

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DichlorophenethylamineHCID 217958—
Reactant1-Methyl-7,8-dihydroquinoline-2,5(1H,6H)-dioneHCID 10442242—
Catalystp-Toluenesulfonic acidHCID 6101—
SolventTolueneHCID 1140—
ProductHCID 10383281HCID 1038328163.9%

Reaction Steps

A mixture of 2-(3,4-dichlorophenyl)ethylamine (3.8 g), 5,6,7,8-tetrahydro-1-methyl-5-oxo-2(1H)-quinolinone (3.0 g), and para-toluenesulfonic acid (130 mg) was heated in refluxing toluene (50 ml), with azeotropic removal of water, for 41 hrs. An additional 1 g of the amine and 0.1 g of para-toluenesulfonic acid were added, and the mixture was heated for an additional 24 hrs. The solution was cooled and the precipitate was collected. Sodium borohydride (0.6 g) was added to a solution of the precipitate in ethyl alcohol (50 ml), and the mixture was stirred at room temperature for 1 hr. The mixture was concentrated in vacuo, the residue was quenched with water, and the mixture was extracted with dichloromethane. The combined organic layers were washed with brine, dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated. The residue was dissolved in hot ethanol and treated with an equivalent amount of fumaric acid. The solid was collected and recrystallized from ethanol to provide 3.8 g (48%) of product, mp 172°-173° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05110815
Source datasetuspto-grants-1992_05
ORD IDord-4f096a598a054ed4b305e4a6811e9f54
Source noteuspto-grants-1992_05