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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254894Generated: October 27, 2026

Trifluoromethanesulfonic acid → N-methoxymethyl-N-methylpyrrolidinium trifluoromethanesulfonate

https://huagongshe.com/reaction/254894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantN-methoxymethyl-N-methylpyrrolidinium chlorideHCID 23116042—
SolventChloroformHCID 6212—
ProductN-methoxymethyl-N-methylpyrrolidinium trifluoromethanesulfonateHCID 8661868095.4%

Reaction Steps

In 116 g of dehydrated chloroform (reagent, Wako Pure Chemical Ind. Ltd.) was dissolved 24.3 g of N-methoxymethyl-N-methylpyrrolidinium chloride. To the solution was added dropwise 24.3 g of trifluoromethane sulfonic acid (reagent, Aldrich Corp.) at 5° C. over a period of 1 hour. The mixture was reacted at room temperature for 2 hours with gradual increase of temperature. The reaction mixture was concentrated and dried in a vacuum. The residue was purified through alumina column (ICN Biomedicals. GmbH, ICN Alumina N, Act.1/eluent acetonitrile). The eluate was concentrated and dried in a vacuum to obtain 39.1 g of the desired product (colorless liquid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875732B2
Source datasetuspto-grants-2011_01
ORD IDord-0aca38ac87b54e4996621794bc5a5aad
Source noteuspto-grants-2011_01