HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 8-Chloro-1,2,3,4,5,6-hexahydrobenzo[f]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 8-chloro-1,4,5,6-tetrahydrobenzo[f]quinolin-3(2H)-one | HCID 10466539 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 8-Chloro-1,2,3,4,5,6-hexahydrobenzo[f]quinoline | HCID 19833134 | — |
Reaction Steps
147 g (1.94 mol) of lithium aluminum hydride were suspended in 4 l of tetrahydrofuran under argon, 454 g (1.94 mol) of 8-chloro-1,4,5,6-tetrahydrobenzo[f]quinolin-3(2H)-one were slowly added thereto and the mixture was boiled under reflux for 2.5 hours. The mixture was then cooled, 470 ml of 18 percent sodium hydroxide solution were added thereto, the resulting mixture was stirred at room temperature for 30 minutes, filtered and the filter residue was washed with tetrahydrofuran. Upon evaporation of the filtrate there was obtained 8-chloro-1,2,3,4,5,6-hexahydrobenzo[f]quinoline as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04732979 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-6474cb477e644736a598c7433bc053b5 |
| Source note | uspto-grants-1988_03 |