HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromide ion → Benzo[b]quinolizinium hexafluorophosphate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | Benzo(b)quinolizinium, bromide (1:1) | HCID 202130 | — |
| Reactant | Potassium hexafluorophosphate | HCID 23688904 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzo[b]quinolizinium hexafluorophosphate | HCID 15186209 | 94.8% |
Reaction Steps
Benzo[b]quinolizinium bromide (508.5 g, 1.95 mol) was dissolved in 5 L of distilled water with heating (steam-bath). Potassium hexafluorophosphate (367.2 g, 1.95 mol) was dissolved in 1.1 L of water with heating and the resulting solution was poured in portions into the above bromide solution with steam-bath heating (20 min). The precipitate was formed immediately and the mixture was stirred at room temperature for 3 h, then stirred 1 h in an ice-water bath. The solid was filtered, washed with cold water (800 mL), dried (50°-60° C.) in vacuo for 3 days to afford 601 g (94.8%) of benzo[b]quinolizinium hexafluorophosphate. (Formula lI: R1 =R2 =R7 =H; X- --=PF6-).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05554620 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-2cdff59ae1c44c3abae0908a3b242acb |
| Source note | uspto-grants-1996_09 |