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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700485Generated: October 31, 2026

Potassium Hydroxide → 7-(2,3-Dichlorophenyl)-4-methyl-5,6,7,8-tetrahydroquinolin-5-one

https://huagongshe.com/reaction/1700485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant1-Amino-5-(2,3-dichlorophenyl)cyclohexen-3-oneHCID 18317446—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product7-(2,3-Dichlorophenyl)-4-methyl-5,6,7,8-tetrahydroquinolin-5-oneHCID 10957724117.1%

Reaction Conditions

Temperature115 °C

Reaction Steps

In a mixture of ethanol (30 ml) and toluene (90 ml) was dissolved 1-amino-5-(2, 3-dichlorophenyl)cyclohexen-3-one (1.5 g), and to the solution were added 3-oxobutylaldehydedimethylacetal (2 g) and granulated potassium hydroxide (330 mg). The mixture was stirred at 115° C. (bath temperature), and to the mixture was added granulated potassium hydroxide (70 mg), 30 minutes later; 1 hour later; and 1.5 hours, respectively. The reaction solution was stirred at the same temperature for 1 hour, cooled and concentrated under reduced pressure, and to the residue were added ethyl acetate (50 ml) and water (20 ml). The mixture was shaken and separated ethyl acetate layer was washed with brine. Under reduced pressure, ethyl acetate was evaporated, and the residue was purified with silica gel column chromatography (EtOAc/hexane) and eluted with ethyl acetate/hexane to give 7-(2,3-dichlorophenyl)-4-methyl-5,6,7,8-tetrahydroquinolin-5-one (1.05 g) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350749B1
Source datasetuspto-grants-2002_02
ORD IDord-74fec995dba34707a9dfd71f13e60f74
Source noteuspto-grants-2002_02