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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537708Generated: October 26, 2026

Hydrochloric Acid → Pyridinium Methanesulfonate

https://huagongshe.com/reaction/537708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetraethoxysilaneHCID 6517—
Reactant1-Ethoxy-2-propanolHCID 15287—
ReactantTriethoxymethylsilaneHCID 16241—
ReactantTrimethoxyphenylsilaneHCID 18137—
ReactantHCID 86654377HCID 86654377—
SolventAcetoneHCID 180—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductPyridinium MethanesulfonateHCID 86654378—

Reaction Steps

4.93 g of phenyltrimethoxysilane, 72.46 g of tetraethoxysilane, 22.06 g of methyltriethoxysilane, 0.56 g of the 30% methanol solution of trimethoxysilylethylmethylpyridinium methanesulfonate, and 150 g of acetone were charged into a 500 mL flask to be dissolved and the resultant mixed solution was warmed while stirring the mixed solution with a magnetic stirrer to reflux. Next, 33.13 g of 0.01 M hydrochloric acid was added to the mixed solution. The mixed solution was subjected to the reaction for 240 minutes and then the resultant reaction solution was cooled down to room temperature. Then, 200 g of propylene glycol monoethyl ether was added to the reaction solution, and ethanol and methanol as reaction by-products, acetone, water, and hydrochloric acid were distilled off under reduced pressure to obtain a hydrolysis-condensation product. The polymer thus obtained corresponded to Formula (VII-21):

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08864894B2
Source datasetuspto-grants-2014_10
ORD IDord-bea5e7d5b0b94727b2bb3d970edd5cb2
Source noteuspto-grants-2014_10