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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781116Generated: October 30, 2026

Hydrogen Peroxide → 1-Acetoxy-4-aza-1-azoniabicyclo[2.2.2]octane tetrafluoroborate

https://huagongshe.com/reaction/1781116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantAcetyl chlorideHCID 6367—
ReactantDabcoHCID 9237—
ReactantSodium TetrafluoroborateHCID 4343483—
Reactant1,4-Diazabicyclo(2.2.2)octane, 1-oxideHCID 11137181—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
Product1-Acetoxy-4-aza-1-azoniabicyclo[2.2.2]octane tetrafluoroborateHCID 19048036—
Product1-acetoxy-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) 1,4-Diazabicyclo[2.2.2]octane N-oxideHCID 86750856—

Reaction Steps

1-acetoxy-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) 1,4-Diazabicyclo[2.2.2]octane N-oxide is prepared by the reaction of 1,4-diazabicyclo[2.2.2]octane with hydrogen peroxide as described by Farkas in J. Chem. Eng. Data (1968) 13,278. 1,4-Diazabicyclo[2.2.2]octane N-oxide (12.8 g, 10 mmol) in THF (100 mL) is reacted with acetyl chloride (7.9 g, 10 mmol) until the reaction is complete by TLC. The reaction is evaporated, diluted with acetonitrile (100 mL) and sodium tetrafluoroborate (40 g, 20 mmol) added. The solution is stirred overnight at room temperature and then filtered to remove all undissolved salts. The flltrate is evaporated to afford 1-acetoxy-4-aza-1-azoniabicyclo[2.2.2]octane tetrafluoroborate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05631372
Source datasetuspto-grants-1997_05
ORD IDord-f9e0c9f2c0c944d59a70ae8393a741c1
Source noteuspto-grants-1997_05