HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1244702Erstellt: 24. Oktober 2026
2-Thiopheneacetic acid → S-[3-(Triethoxysilyl)propyl] ethanethioate
https://huagongshe.com/de/reaction/1244702
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Thiopheneacetic acid | HCID 15970 | — |
| Edukt | (3-Chloropropyl)triethoxysilane | HCID 78771 | — |
| Edukt | Sodium ethoxide | HCID 2723922 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | 2-Thiophenecarboxylic acid | HCID 10700 | — |
| Produkt | S-[3-(Triethoxysilyl)propyl] ethanethioate | HCID 21922028 | 78% |
Reaktionsschritte
This example illustrates the preparation of a thiocarboxylate alkoxysilane from a salt of a thiolcarboxylic acid using as a solvent the alcohol corresponding to the silane alkoxy group. Into a 250 ml, three-neck round bottomed flask equipped with magnetic stir bar, temperature probe/controller, heating mantle, addition funnel, condenser, and N2 inlet was charged 63 grams of a 21 weight percent sodium ethoxide in ethanol. Fifteen grams of thiolacetic acid was added slowly, keeping the temperature below 65° C. The solution was allowed to cool to room temperature, and 48 grams of chloropropyltriethoxysilane was added via the addition funnel. After addition was complete, the solution was heated to 70° C. for 24 hours whereupon a white solid formed. Analysis of the solution by gas chromatography showed a 78 percent yield of acetylthiopropyltriethoxysilane.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07122590B2 |
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| Quelldatensatz | uspto-grants-2006_10 |
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| ORD ID | ord-3910189f7bc84d7493667a0e713c210c |
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| Quellennotiz | uspto-grants-2006_10 |
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