HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → 1-Acetoxy-4-aza-1-azoniabicyclo[2.2.2]octane tetrafluoroborate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | Sodium Tetrafluoroborate | HCID 4343483 | — |
| Reactant | 1,4-Diazabicyclo(2.2.2)octane, 1-oxide | HCID 11137181 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Acetoxy-4-aza-1-azoniabicyclo[2.2.2]octane tetrafluoroborate | HCID 19048036 | — |
| Product | 1-acetoxy-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) 1,4-Diazabicyclo[2.2.2]octane N-oxide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05631372 |
| Source dataset | uspto-grants-1997_05 |
| ORD ID | ord-f9e0c9f2c0c944d59a70ae8393a741c1 |
| Source note | uspto-grants-1997_05 |