HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641922Generated: October 25, 2026
Potassium Nitrate → 5-Bromo-8-nitroisoquinoline
https://huagongshe.com/reaction/641922
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | 5-Bromoisoquinoline | HCID 736487 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 5-Bromo-8-nitroisoquinoline | HCID 816983 | — |
Reaction Steps
Into a 500 mL 3-necked round bottom flask was placed a solution of 5-bromoisoquinoline (22.24 g, 106.87 mmol) in H2SO4 (120 mL). This was followed by the addition of a solution of KNO3 (15.1 g, 149.36 mmol) in H2SO4 (100 mL), which was added dropwise with stirring, while cooling to a temperature of 20° C. over a time period of 1 hour. The resulting solution was allowed to react, with stirring, for 1 hour while the temperature was maintained at room temperature. The reaction progress was monitored by TLC (ethyl acetate/petroleum ether=1:5). The reaction mixture was then quenched by the adding 600 mL of H2O/ice. Adjustment of the pH to 8-10 was accomplished by the addition of NH3. H2O (30%). A filtration was performed. The filter cake was washed 2 times with 500 mL of H2O. The solid was dried in an oven under reduced pressure. This resulted in 25.59 g (90%) of 5-bromo-8-nitroisoquinoline as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696229B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-7db5e9af87b84bd0b93bea6e49f41bd0 |
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| Source note | uspto-grants-2010_04 |
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