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HRID 1244702作成日:2026年10月27日

2-Thiopheneacetic acid → S-[3-(Triethoxysilyl)propyl] ethanethioate

https://huagongshe.com/reaction/1244702

反応式

関与物質

役割名称HCID仕込み量
反応物2-Thiopheneacetic acidHCID 15970—
反応物(3-Chloropropyl)triethoxysilaneHCID 78771—
反応物Sodium ethoxideHCID 2723922—
溶媒EthanolHCID 702—
溶媒2-Thiophenecarboxylic acidHCID 10700—
生成物S-[3-(Triethoxysilyl)propyl] ethanethioateHCID 2192202878%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07122590B2
出典データセットuspto-grants-2006_10
ORD IDord-3910189f7bc84d7493667a0e713c210c
出典メモuspto-grants-2006_10