HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452113Generated: October 28, 2026
Hydrogen Peroxide → 1-Fluoro-4-hydroxy-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate)
https://huagongshe.com/reaction/1452113
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | Fluorine | HCID 24524 | — |
| Reactant | Tetrafluoroboric acid | HCID 28118 | — |
| Product | 1-Fluoro-4-hydroxy-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) | HCID 2737329 | 93% |
Reaction Steps
To a solution of 1,4-diazabicyclo[2.2.2]octane (11.2 g, 0.1 mole) in water (100 mL) was added 30% hydrogen peroxide (22.8 mL) while maintaining the temperature between 15°and 20° C. The reaction was stirred at room temperature (20-22° C.) overnight. Next, boron trifluoride gas (6.8 g, 0.1 mole) and tetrafluoroboric acid (50% solution, 10 mL, 0.1 mole) were added, the solution cooled to 9° C. and treated with a mixture of fluorine in nitrogen (10% V/V, 0.125 mole). The reaction was evaporated, the remaining solid washed with acetone and dried to afford 30 grams of 1-hydroxyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (93% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05606084 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-26dedc844817457ea006039257759cb3 |
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| Source note | uspto-grants-1997_02 |
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