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Ethyl trimethylsilylacetate → [1-[5-(4-Fluorobenzyl)furan-2-yl]vinyloxy]-trimethylsilane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl trimethylsilylacetate | HCID 77687 | — |
| 反応物 | 1-[5-[(4-Fluorophenyl)methyl]-2-furanyl]ethanone | HCID 10130640 | — |
| 触媒 | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | [1-[5-(4-Fluorobenzyl)furan-2-yl]vinyloxy]-trimethylsilane | HCID 21972883 | 88% |
反応手順
A solution of 2-acetyl-5-(4-fluorobenzyl)furan (10 g, 46 mmol) and trimethylsilylacetic acid ethyl ester (10.9 g, 68 mmol) in anhydrous THF (30 ml) was cooled at −20° C. To a solution was added anhydrous tetrabutylammoniumfluoride (0.2 g). The reaction mixture was gradually warmed up to room temperature and stirred for 15 minutes at 50° C. The THF was evaporated under reduced pressure. The residue was distilled under reduced pressure. The fraction showing b.p. 130° C. (0.5 mmHg) was collected to give [1-[5-(4-fluorobenzyl)furan-2-yl]vinyloxy]-trimethylsilane (11.7 g). Yield 88%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07098201B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-719ecd62b0b94a0fbbe448ddbdc6e91c |
| 出典メモ | uspto-grants-2006_08 |