HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propynal → 5(6H)-Quinolinone, 7,8-dihydro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propynal | HCID 12222 | — |
| Reactant | 3-Aminocyclohex-2-en-1-one | HCID 78892 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5(6H)-Quinolinone, 7,8-dihydro- | HCID 3016811 | 54.2% |
Reaction Steps
The procedure of Rimek and Zymalkowski (Arch. Pharm. 1961, 294, 759-765) was followed. Over a period of 1 hour, 40.9 g (0.757 mol) of freshly-distilled propiolaldehyde was added dropwise to a solution of 42.1 g (0.379 mol) of 3-amino-2-cyclohexenone in 1.5 1 of N,N-dimethylformamide (DMF). The solution was stirred at room temperature for 12 hours. The DMF was evaporated at reduced pressure. Vacuum distillation (bp 60°-65° C. at 0.025-0.050 mmHg) of the resultant black tars gave 30.2 g (54.2%) of 7,8-dihydro-5(6H)-quinolinone as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04762843 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-d095c268899d483fbe6ef5a5fd78e336 |
| Source note | uspto-grants-1988_08 |