HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537695Generated: October 31, 2026
Methyl Methanesulfonate → Trimethoxysilylpropyltrimethylammonium methanesulfonate
https://huagongshe.com/reaction/537695
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Methanesulfonate | HCID 4156 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-Propanamine, N,N-dimethyl-3-(trimethoxysilyl)- | HCID 75668 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Trimethoxysilylpropyltrimethylammonium methanesulfonate | HCID 86654371 | — |
Reaction Steps
5.0 g of trimethoxysilylpropyldimethylamine and 24 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 3.0 g of methyl methanesulfonate was dissolved in 26 g of ethanol was gradually added at room temperature in a nitrogen atmosphere. The reaction mixture was stirred for half a day and therefrom, ethanol was distilled off under reduced pressure. The resultant concentrate was dropped into 100 mL of diethyl ether and therefrom, trimethoxysilylpropyldimethylamine 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 ethanol to obtain a 38.1% ethanol solution of trimethoxysilylpropyltrimethylammonium methanesulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08864894B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-4f0d54311a154482808de1ec2e6bedca |
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| Source note | uspto-grants-2014_10 |
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