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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537707Generated: October 29, 2026

Methyl Methanesulfonate → HCID 86654377, compound

https://huagongshe.com/reaction/537707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl MethanesulfonateHCID 4156—
Reactant2-(Trimethoxysilylethyl)pyridineHCID 2760506—
SolventEthyl AcetateHCID 8857—
ProductHCID 86654377HCID 86654377—

Reaction Steps

5.0 g of 2-(trimethoxysilylethyl)pyridine and 18 g of ethyl acetate were charged into a 100 mL flask to be dissolved. While stirring the resultant mixed solution with a magnetic stirrer, to the mixed solution, a solution in which 3.6 g of methyl methanesulfonate was dissolved in 24 g of ethyl acetate was gradually added at room temperature in a nitrogen atmosphere. The reaction mixture was refluxed over 3 days and therefrom, ethyl acetate was distilled off under reduced pressure. The resultant concentrate was dropped into 100 mL of diethyl ether and therefrom, 2-(trimethoxysilylethyl)pyridine and methyl methanesulfonate as by-products were removed. This purification was repeated three times and then remaining diethyl ether was distilled off under reduced pressure, followed by dissolving the resultant concentrate in methanol to obtain a 30% methanol solution of trimethoxysilylethylmethylpyridinium methanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08864894B2
Source datasetuspto-grants-2014_10
ORD IDord-9aa9d2637d92437493cf34c8c67db34c
Source noteuspto-grants-2014_10