Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| 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 as a nonprotic solvent. 88 grams of powdered sodium ethoxide and 600 ml diglyme were charged into a 1 liter, 3 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 3 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 |
|---|
| Patent number | US06414061B1 |
|---|
| Source dataset | uspto-grants-2002_07 |
|---|
| ORD ID | ord-106ec93ad3044acdac3aa72599296245 |
|---|
| Source note | uspto-grants-2002_07 |
|---|