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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906118Generated: November 1, 2026

Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1) → HCID 178483340, compound

https://huagongshe.com/reaction/1906118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxonium, trimethyl-, tetrafluoroborate(1-) (1:1)HCID 2735153—
Reactantcyclopenta-1,3-diene;1-cyclopenta-2,4-dien-1-yl-N,N-dimethylmethanamine;iron(2+)HCID 15764045—
SolventDichloromethaneHCID 6344—
ProductHCID 178483340HCID 178483340—

Reaction Steps

(Trimethylammoniomethyl)ferricinium bis(tetrafluoroborate) was prepared by the following procedure. A slurry of 7.47 g of trimethyloxonium tetrafluoroborate (50.6 mmol) in 125 mL of CH2Cl2 was added to 10 mL of dimethylaminomethylferrocene in 100 mL of the same solvent. The resulting mixture was stirred for 16 hours and the solvent was removed under reduced pressure. The resulting residue was recrystallized from hot water to give 13.62 g of (trimethylammoniomethyl)ferrocene tetrafluoroborate as golden-yellow platelets. 1.32 g of the (trimethylammoniomethyl)ferrocene tetrafluoroborate (8 mmol) were added to a mixture of 0.864 g of p-benzoquinone (8 mmol) and 2.16 mL of 48% aqueous tetrafluoroboric acid (16 mmol) in 60 mL of diethyl ether. The resulting mixture was stirred for 15 minutes and filtered to give a dark blue-black residue which was washed with ether until the washings were colorless to remove quinhydrone and dried under reduced pressure to give 1.69 g of (trimethyl-ammoniomethyl)ferricinium bis(tetrafluoroborate) (3.9 mmol) as a navy-blue solid, which decomposed at high temperature without a characteristic melting point.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04650609
Source datasetuspto-grants-1987_03
ORD IDord-75a8e90fb05f401a87fc18ed9391de01
Source noteuspto-grants-1987_03