HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrafluoroboric acid → HCID 178433651, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Reactant | HCID 178432781 | HCID 178432781 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178433651 | HCID 178433651 | — |
Reaction Steps
0.86 g of 1-benzylideneamino-2,3-dimethylimidazolium tetrafluoroborate is suspended in 30 ml of water. The suspension is treated with 1 ml of 50 percent tetrafluoroboric acid and steam-distilled until benzaldehyde no longer passes over. The colorless acidic solution is then treated with 0.45 g of p-(dimethylamino)benzaldehyde and stirred at room temperature for 3 hours. The resulting orange-yellow precipitate is removed by filtration under suction, washed three times with water and three times with diethyl ether and recrystallized from methanol/ethanol. There is obtained 1-[[p-(dimethylamino)benzylidene[amino[-2,3-dimethylimidazolium tetrafluoroborate in the form of yellow needles with a melting point of 248°-251°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04956470 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-2d309a2a5fe449678d93d5ddeac5de0c |
| Source note | uspto-grants-1990_09 |