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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286463Generated: October 25, 2026

Epichlorohydrin → 2-Ethoxy-1-methylquinolinium fluoroborate

https://huagongshe.com/reaction/2286463

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantBoron trifluoride etherateHCID 8000—
Reactant1-Methyl-2-quinoloneHCID 11820—
ReactantTriethyloxonium tetrafluoroborateHCID 2723982—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductTriethyloxonium tetrafluoroborateHCID 2723982—
Product2-Ethoxy-1-methylquinolinium fluoroborateHCID 1305945483.5%

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 fluoroborate is dissolved in 20 ml of dry methylene chloride and treated under nitrogen with 6.47 g (0.040 mole) of N-methyl-2-quinolone in 15 ml of methylene chloride. The reaction mixture is stirred under nitrogen at room temperature overnight. The solid is filtered to give 9.2 g (83.5%) of 2-ethoxy-1-methylquinolinium fluoroborate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04266062
Source datasetuspto-grants-1981_05
ORD IDord-b35aa481d3e54da7ab217650a0e7c1be
Source noteuspto-grants-1981_05