HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860290Generated: October 27, 2026
2-Thiophenecarboxylic acid → Acetylthiomethyltriethoxysilane
https://huagongshe.com/reaction/1860290
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Thiophenecarboxylic acid | HCID 10700 | — |
| Reactant | 2-Thiopheneacetic acid | HCID 15970 | — |
| Reactant | Silane, (chloromethyl)triethoxy- | HCID 84858 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | Acetylthiomethyltriethoxysilane | HCID 12135714 | 55% |
Reaction Steps
This example illustrates the preparation of a thiocarboxylate alkoxysilane from a salt of a thiolcarboxylic acid using a nonprotic solvent. 88 grams of powdered sodium ethoxide and 600 ml diglyme were charged into a one-liter, three-neck round bottomed flask equipped with magnetic stir bar, temperature probe/controller, heating mantle, addition funnel, condenser, N2 inlet, and ice water bath. The solution was cooled to 8° C., and 105 grams of thiolacetic acid was added slowly via the addition funnel, keeping the temperature below 60° C. The solution was allowed to cool to 35° C., and 250 grams of chloromethyltriethoxysilane was added via the addition funnel. After addition was complete, the solution was heated to 70° C., where a brief exotherm to 120° C. was observed. The solution was heated at 70° C. for an additional three hours. A white solid formed which was filtered first through a 0.1 μm pressure filter and then a 0.01 μm filter to give a clear, black solution. The solvent was removed under reduced pressure, and the remaining liquid vacuum distilled to yield 163 grams of a clear and colorless liquid, a 55 percent yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06528673B2 |
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| Source dataset | uspto-grants-2003_03 |
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| ORD ID | ord-974a051d06df48c9a774f91daef9eb20 |
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| Source note | uspto-grants-2003_03 |
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