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 are 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 are slowly added thereto and the mixture is boiled under reflux for 2.5 hours. The mixture is then cooled and 470 ml of 18 percent sodium hydroxide solution are added thereto. The resulting mixture is stirred at room temperature for 30 minutes, filtered and the filter residue is washed with tetrahydrofuran. Upon evaporation of the filtrate, there is 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 | US04883815 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-4376940c6975428b81b56d399235fbb7 |
| Source note | uspto-grants-1989_11 |