HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-Acetyl-8-chloro-1,1-dimethyl-1,2,3,4,5,6-hexahydrobenzo[f]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acetyl bromide | HCID 10482 | — |
| Reactant | 8-Chloro-1,1-dimethyl-1,2,3,4,5,6-hexahydrobenzo[f]quinoline | HCID 19833128 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Acetyl-8-chloro-1,1-dimethyl-1,2,3,4,5,6-hexahydrobenzo[f]quinoline | HCID 19833157 | — |
Reaction Steps
10.6 g (0.043 mol) of 8-chloro-1,1-dimethyl-1,2,3,4,5,6-hexahydrobenzo[f]quinoline and 6.6 ml (0.047 mol) of triethylamine are dissolved in 100 ml of methylene chloride and 3.5 ml (0.047 mol) of acetyl bromide dissolved in 20 ml of methylene chloride are added dropwise thereto at 0°. After stirring for 1 hour, the mixture is extracted with methylene chloride/water, dried with magnesium sulfate and the solvent is distilled in a vacuum. Recrystallization from methylene chloride/hexane gives 4-acetyl-8-chloro-1,1-dimethyl-1,2,3,4,5,6-hexahydrobenzo[f]quinoline as white crystals with melting point 126°-127°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04883815 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-46f97af6a566466b93d3f09a2110e922 |
| Source note | uspto-grants-1989_11 |