HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → 6-Butylbenzo[b]quinolizinium perchlorate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Benzo(b)quinolizinium, bromide (1:1) | HCID 202130 | — |
| Reactant | Sodium Perchlorate | HCID 522606 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | 6-Butylbenzo[b]quinolizinium perchlorate | HCID 19047476 | — |
Reaction Steps
A solution of KCN (3g, 0.046 mol) in a minimum of water was added to a solution of benzo[b]quinolizinium bromide (10 g; 0.0385 mol) in 200 ml water. The resulting solid was extracted with an equal volume of methylene chloride. The above organic layer was heated and a solution of bromine (6.4 g) in methylene chloride was added. The resulting yellow solid was isolated, dissolved in ethanol/water, and the resulting solution was treated with sodium perchlorate solution. The perchlorate salt was filtered and recrystallized from ethanol to afford 2 g of 6-cyano-benzo[b]quinolizinium perchlorate (Formula II: R1 =R7 =H; R2 =CN; X- =ClO4-) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05631264 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-a996c746ecb54471ac6df38e30d8d3e1 |
| Source note | uspto-grants-1997_05 |