HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrolein → 3-Chloro-7,8-dihydroquinolin-5(6H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrolein | HCID 7847 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2,3-Dichloro-2-propenal | HCID 150516 | — |
| Reactant | 3-Aminocyclohexan-1-one | HCID 21873184 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Chloro-7,8-dihydroquinolin-5(6H)-one | HCID 10997654 | — |
Reaction Steps
In reaction 3 of Scheme 1, a solution of oxalyl chloride in methylene chloride is added dropwise to a solution of chloromalondialdehyde III in methyene chloride and a phase transfer catalyst, such as dimethylformamide, under inert reaction conditions. The reaction mixture is stirred at room temperature until conversion to the corresponding 2,3-dichloroacrolein is complete. In reaction 4 of Scheme 1, a solution of 1-amino-cyclohexan-3-one VI in dimethylformamide is added dropwise to the above acrolein to form the corresponding 3-chloro-5,6,7,8-tetrahydroquinolin-5-one VII. The reaction, generally carried out overnight, will be in the temperature range between about 60° C. to about 80° C., preferably about 70° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05206367 |
| Source dataset | uspto-grants-1993_04 |
| ORD ID | ord-4de99e44c85c41d488652a206de3a760 |
| Source note | uspto-grants-1993_04 |