HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-Methyl-7,8-dihydroquinolin-5(6H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Cyclohexanedione | HCID 10434 | — |
| Reactant | 3-Ethoxy-2-methyl-2-propenal | HCID 559198 | — |
| Catalyst | Ammonium Acetate | HCID 517165 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Methyl-7,8-dihydroquinolin-5(6H)-one | HCID 595192 | 48% |
Reaction Steps
A mixture of cyclohexane-1,3-dione (11.2 g. 0.1 m), 3-amino-2-methylacrolein (8.5 g. 0.1m) triethylamine (5 ml.) and ammonium acetate (100 mg) were heated with stirring at 120° in an oil bath for 12 hours. The cooled reaction mixture was diluted with ether (50 ml.) and the solution washed with 2N HCl (3 × 15 ml.) The combined washings were adjusted to pH 9.0 with sodium carbonate and extracted with ether (3 × 50 ml.) The combined extracts were dried, evaporated in vacuo and the residual oil distilled at 0.2 mm Hg to give the title compound as a colourless crystalline solid b.p. 80° (7.5 g. 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03998831 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-51b4b626a0284eb0a20fab8c3fa7139f |
| Source note | uspto-grants-1976_12 |