HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 3,4-Dihydroxy-5-nitrophenyl (3-quinolinyl) ketone hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 4-Hydroxy-3-methoxy-5-nitrophenyl (3-quinolinyl) ketone | HCID 19000153 | — |
| Product | 3,4-Dihydroxy-5-nitrophenyl (3-quinolinyl) ketone hydrobromide | HCID 19000163 | — |
Reaction Steps
820 mg of 4-hydroxy-3-methoxy-5-nitrophenyl (3-quinolinyl) ketone are treated with 50 ml of 48 percent hydrobromic acid and held at the reflux temperature for 3 hours. After distillation of the hydrobromic acid at 50°, the residue is treated with 70 ml of hot water and the insoluble constituent is filtered under suction. There is obtained 3,4-dihydroxy-5-nitrophenyl (3-quinolinyl) ketone hydrobromide in the form of yellow crystals of m.p. 270° (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05633371 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-4fc45fe431c548d7b426c04fca9717f0 |
| Source note | uspto-grants-1997_05 |