HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Anisoyl chloride → 4-(p-Methoxybenzoyl)-8-chloro-1,2,3,4,5,6-hexahydrobenzo[f]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 8-Chloro-1,2,3,4,5,6-hexahydrobenzo[f]quinoline | HCID 19833134 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(p-Methoxybenzoyl)-8-chloro-1,2,3,4,5,6-hexahydrobenzo[f]quinoline | HCID 19833152 | — |
Reaction Steps
15.0 g (0.06 mol) of 8-chloro-1,2,3,4,5,6-hexahydrobenzo[f]quinoline were dissolved in 150 ml of methylene chloride, treated with 6.68 g (0.066 mol) of triethylamine and 11.2 g (0.066 mol) of p-methoxybenzoyl chloride in 50 ml of methylene chloride were added dropwise thereto at 0°. After stirring at room temperature for 1 hour the mixture was extracted with water, dried with magnesium sulphate and the solvent was distilled off in vacuo. Crystallization (methylene chloride-ether) gave 4-(p-methoxybenzoyl)-8-chloro-1,2,3,4,5,6-hexahydrobenzo[f]quinoline as white crystals of melting point 182°-183°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04732979 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-2a0e0e0e08d847f0a132f44f8b922dbc |
| Source note | uspto-grants-1988_03 |