HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphorus oxychloride → 4-Chlorobenzo[g]quinoline-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 4-Oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrile | HCID 9834413 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Product | 4-Chlorobenzo[g]quinoline-3-carbonitrile | HCID 9834630 | 49.5% |
Reaction Steps
A reaction mixture of 3.5 g (16 mmol) of 4-oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrile in 35 mL of phosphorus oxychloride and 22 drops of N,N-dimethylformamide (DMF) is heated at 100–110° C. for 5 hours. After cooling, the mixture is concentrated to dryness in vacuo to give a dark residue. The residue is partitioned between methylene chloride and ice-cooled saturated aqueous sodium carbonate solution. The organic layer is washed with ice-cooled brine and dried over sodium sulfate. The organic solvent is passed through a short column of silica gel, and further eluted with additional methylene chloride. Removal of the solvent yields 1.89 g (49.5%) of the product as a bright yellow solid, mp 253–255° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105531B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-8298d1868b904d48ab9dc49d0e6c4ece |
| Source note | uspto-grants-2006_09 |