Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781122Generated: November 4, 2026

Methanesulfonyl chloride → HCID 19048030, compound

https://huagongshe.com/reaction/1781122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium TetrafluoroborateHCID 4343483—
ReactantHCID 86750858HCID 86750858—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19048030HCID 19048030—

Reaction Steps

1-Fluoro-4-methanesulfonyl-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) 1,4-Diazabicyclo[2.2.2]octane (11 g, 10 mmol) in tetrahydrofuran (100 mL) is reacted with methanesulfonyl chloride (11.5 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 filtrate is evaporated to afford 1-methanesulfonyl-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-7aa01f68f6ca4bfb93c17f6e95f142b9
Source noteuspto-grants-1997_05