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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032050Generated: October 31, 2026

Tetrafluoroboric acid → HCID 178433651, compound

https://huagongshe.com/reaction/1032050

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrafluoroboric acidHCID 28118—
ReactantHCID 178432781HCID 178432781—
SolventWaterHCID 962—
ProductHCID 178433651HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04956470
Source datasetuspto-grants-1990_09
ORD IDord-2d309a2a5fe449678d93d5ddeac5de0c
Source noteuspto-grants-1990_09