HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756714Generated: October 28, 2026
Orthosilicic acid → Tetrakis(N,N,N-trimethylmethanaminium) orthosilicate
https://huagongshe.com/reaction/1756714
Participants
| Role | Name | HCID | Charge |
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| Reactant | Orthosilicic acid | HCID 14942 | — |
| Reactant | Tetramethylammonium hydroxide | HCID 60966 | — |
| Product | Tetrakis(N,N,N-trimethylmethanaminium) orthosilicate | HCID 71310495 | — |
Reaction Steps
About 1250 ml of 10% aqueous tetramethylammonium hydroxide solution are added to 82.2 g of precipitated silicic acid. After the mixture has been stirred at 25° C. for 16 hours and at 50° C. for 8 hours, a clear solution is obtained. The solution is concentrated to two thirds of its starting volume and the resulting tetramethylammonium silicate is crystallized at 4° C. About 359.5 g of tetramethylammonium silicate which still contains water are obtained. About 160 g of tetramethylammonium silicate are added in portions to a well-stirred mixture containing 400 ml of water, 1000 ml of isopropanol, 1500 ml (1136 g) of 1,1,3,3-tetramethyldisiloxane (obtained under the name "HSi2" from Wacker-Chemie GmbH, D-8000 Munich) and 200 ml of 10% hydrochloric acid and the reaction mixture is then stirred at room temperature for 4 hours. The phases are then separated and the organic phase is washed with water until neutral, dried over sodium sulfate and evaporated completely. The residue is recrystallized from acetone. About 52.0 g of octa(hydrogendimethylsiloxy)octasilsesquioxane are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05442025 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-6fec402e6c69478db5e1662bbb64e27d |
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| Source note | uspto-grants-1995_08 |
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