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HRID 396929作成日:2026年10月24日

2-Thiophenecarboxylic acid → Acetylthiomethyltriethoxysilane

https://huagongshe.com/ja/reaction/396929

反応式

関与物質

役割名称HCID仕込み量
反応物2-Thiophenecarboxylic acidHCID 10700—
反応物2-Thiopheneacetic acidHCID 15970—
反応物Silane, (chloromethyl)triethoxy-HCID 84858—
反応物Sodium ethoxideHCID 2723922—
溶媒DiglymeHCID 8150—
生成物AcetylthiomethyltriethoxysilaneHCID 1213571455%

反応条件

温度8 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06608125B2
出典データセットuspto-grants-2003_08
ORD IDord-ce850b0c132b4594a4b26de67431649d
出典メモuspto-grants-2003_08