HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 3-[(2-Naphthyloxy)methyl][1,4]benzodioxino[2,3-c]pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 2-Naphthol | HCID 8663 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(Bromomethyl)[1,4]benzodioxino[2,3-c]pyridazine | HCID 117691171 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[(2-Naphthyloxy)methyl][1,4]benzodioxino[2,3-c]pyridazine | HCID 89584645 | 65.2% |
Reaction Steps
To 3-(bromomethyl)[1,4]benzodioxino[2,3-c]pyridazine (500 mg) were added dimethylformamide (10 ml), potassium iodide (30 mg), potassium carbonate (750 mg) and 2-naphthylalcohol (290 mg), and the mixture was stirred at room temperature for 24 hr. Water was added and the mixture was extracted with ethyl acetate. The organic layer was washed with 1M aqueous sodium hydroxide solution and saturated brine, and dried over anhydrous sodium sulfate. The solvent was concentrated under reduced pressure, and the residue was washed with diethyl ether and the resulting solid was filtered and dried under reduced pressure to give 3-[(2-naphthyloxy)methyl][1,4]benzodioxino[2,3-c]pyridazine (400 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09212147B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-e3dbc379b74e477098d14e3a13ff124f |
| Source note | uspto-grants-2015_12 |