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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286462Generated: October 27, 2026

Epichlorohydrin → 2-Ethoxy-1-methylpyridinium fluoroborate

https://huagongshe.com/reaction/2286462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantBoron trifluoride etherateHCID 8000—
Reactant1-Methyl-2(1H)-pyridinoneHCID 12755—
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductTriethyloxonium tetrafluoroborateHCID 2723982—
Product2-Ethoxy-1-methylpyridinium fluoroborateHCID 1305945671%

Reaction Steps

Triethyloxonium fluoroborate is prepared from 3.70 g (0.040 mole) of epichlorohydrin in 14 ml of ether and 7.58 g (0.054 mole) of boron trifluoride etherate in 6 ml of ether. The resulting solid triethyloxonium tetrafluoroborate is dissolved in 20 ml of dry methylene chloride and treated under nitrogen with 4.36 g (0.040 mole) of 1-methyl-2-pyridone in 15 ml of methylene chloride. The reaction mixture is stirred under nitrogen at room temperature overnight (about 16 hours). The solvent is evaporated at room temperature, in vacuo and the quaternary salt obtained is recrystallized from methanol-ether (1:1) to give 8.0 g (71%) of 2-ethoxy-1-methylpyridinium fluoroborate, m.p. 58°-60° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04266062
Source datasetuspto-grants-1981_05
ORD IDord-525658bee8e34f7ebb8af4156b889d6e
Source noteuspto-grants-1981_05