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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264104Generated: October 31, 2026

Sodium thiocyanate → N-ethyl-N-methoxymethylpyrrolidinium thiocyanate

https://huagongshe.com/reaction/2264104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium thiocyanateHCID 516871—
ReactantN-ethyl-N-methoxymethylpyrrolidinium chlorideHCID 23116096—
SolventEthanolHCID 702—
ProductN-ethyl-N-methoxymethylpyrrolidinium thiocyanateHCID 8663905488.6%

Reaction Steps

In 140 g of ethanol was dissolved 27.1 g of sodium thiocyanate (reagent, Wako Pure Chemical Ind. Ltd.). In 20.0 g of ethanol was dissolved 40.0 g of N-ethyl-N-methoxymethylpyrrolidinium chloride. The latter solution was added dropwise to the former solution at room temperature over a period of 0.5 hour to perform salt exchange. The mixture was stirred at room temperature for 36 hours to complete the reaction and filtered. The resulting solid product was washed with 300 g of ethanol. The filtrate was dried at reduced pressure. To the resulting product was added 200 ml of dehydrated chloroform (reagent, Wako Pure Chemical Ind. Ltd.) and cooled to −25° C. The mixture was filtered, concentrated and dried in 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 vacuum to obtain 39.9 g of the desired product (colorless liquid). The product was checked for 1H-NMR and electrical conductivity as in Example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07854854B2
Source datasetuspto-grants-2010_12
ORD IDord-291f0478815e4d95812b139eb9d69b4c
Source noteuspto-grants-2010_12