HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 6-Chloro-3-methylaminomethylene-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | 6-Chloro-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline | HCID 14501422 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 6-Chloro-3-methylaminomethylene-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline | HCID 54228418 | 86.1% |
Reaction Steps
A solution of 6-chloro-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline (2 g), N,N-dimethylformamide dimethyl acetal (7.009 g), and triethylamine (0.87 g) in benzene (50 m) was refluxed with stirring for 1 hour and then about three-fourths of the solvent was distilled slowly at atmospheric pressure over a period ximately 1 hour. To the residue was added benzene (100 ml) and the solvent was distilled again. The resulting solid was collected by filtration, washed with diethyl ether, and dried to give 6-chloro-3-methylaminomethylene-4-oxo-1-propionyl-1,2,3,4-tetrahydroquinoline (2.02 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04767780 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-a0798f33254e49d4856614cee3bd6850 |
| Source note | uspto-grants-1988_08 |