HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetylacetone → 7-(5-Fluoro-2-methylphenyl)-2,4-dimethyl-5,6,7,8-tetrahydroquinolin-5-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetylacetone | HCID 31261 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 5-(5-Fluoro-2-methylphenyl)cyclohexane-1,3-dione | HCID 18317771 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 7-(5-Fluoro-2-methylphenyl)-2,4-dimethyl-5,6,7,8-tetrahydroquinolin-5-one | HCID 17823922 | 62.2% |
Reaction Steps
A mixture of 5-(5-fluoro-2-methylphenyl)-cyclohexane-1,3-dione (1.5 g) and ammonium acetate (1.6 g) in butanol(30 ml) was combined with acetylacetone (2.0 g) and heated under reflux for 3 days. The solvent was distilled off under reduced pressure, and the residue was dissolved in ethyl acetate, washed successively with aqueous sodium hydrogen carbonate, water and saturated brine, and dried over magnesium sulfate. The mixture was concentrated under reduced pressure, and the residue was subjected to a column chromatography on a silica gel (ethyl acetate-hexane) to obtain 7-(5-fluoro-2-methylphenyl)-2,4-dimethyl-5,6,7,8-tetrahydroquinolin-5-one (1.2 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06706732B1 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-5ba56389a6444e2d83fa92269cfceb15 |
| Source note | uspto-grants-2004_03 |