HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → HCID 21567739, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 21567798 | HCID 21567798 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21567739 | HCID 21567739 | — |
Reaction Steps
9.2 g of 6-bromo-7-amino-2,3-dihydro-1H-pyrrolo[1,2-a]benzimidazole are dissolved in a mixture of 30 cm3 of water and 9 cm3 of hydrochloric acid. Diazotation is carried out with a solution of 2.5 g of sodium nitrite in 15 cm3 of water. The diazonium salt is neutralized with sodium carbonate and while stirring poured into a solution of 6.89 g of cuprous cyanide and 12.3 g of potassium cyanide in 100 cm3 of water. Stirring is continued for 30 min at room temperature and a further 15 min on a water-bath at 50° to 60°C. After cooling, the precipitate is sucked off. The base is purified by sublimation (200°C/2mm Hg) and recrystallized from a mixture of benzene and n-hexane. Melting point: 224°C. Yield: 4.7 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03931156 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-262df3c6e1664d4cafc441aaec18e865 |
| Source note | uspto-grants-1976_01 |