HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → 5-Bromo-8-nitroisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | 5-Bromoisoquinoline | HCID 736487 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 5-Bromo-8-nitroisoquinoline | HCID 816983 | 96% |
Reaction Steps
A solution of potassium nitrate (1.78 g, 8.56 mmol) was added slowly to a solution of 5-bromoisoquinoline in 12 mL H2SO4. After stirring for 3 hours the reaction mixture was poured onto ice and neutralised with conc. ammonium hydroxide. The yellow precipitate was extracted with ethyl acetate (3×), and the combined organic layers were washed with saturated NaCl, dried over MgSO4, filtered and concentrated. The residue was chromatographed on silica gel (40% ethyl acetate in hexane as eluent) to give 5-bromo-8-nitroisoquinoline in 96% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06693111B1 |
| Source dataset | uspto-grants-2004_02 |
| ORD ID | ord-637bc4b292a3434eb691cfa2ee40aad8 |
| Source note | uspto-grants-2004_02 |