化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1985963作成日:2026年10月27日
2,2,2-Trifluoroacetaldehyde hydrate → 4,4,4-Trifluoro-2-(2,2,2-trifluoroethyl)but-2-enoic acid ethyl ester
https://huagongshe.com/reaction/1985963
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2,2,2-Trifluoroacetaldehyde hydrate | HCID 2781366 | — |
| 反応物 | 4,4,4-Trifluoro-2-(triphenyl-lambda5-phosphanylidene)-butyric acid ethyl ester | HCID 44541424 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4,4,4-Trifluoro-2-(2,2,2-trifluoroethyl)but-2-enoic acid ethyl ester | HCID 74410056 | 86% |
反応手順
To a solution of 4,4,4-trifluoro-2-(triphenyl-λ5-phosphanylidene)-butyric acid ethyl ester (2.0 g, 4.65 mmol) in THF (5 mL) was added 1 mL of trifluoroacetaldehyde hydrate (tech.). The mixture was sealed in a pressure tube and heated at 100° C. for 3.5 h. After cooling to 23° C., the reaction mixture was eluted through a pad of silica gel (100 g) and Na2SO4 with Et2O (100 mL) to remove the by-products triphenylphosphine oxide and water. The eluent was distilled to remove Et2O and to afford the product as a colorless liquid (1.0 g, 86%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07547725B2 |
|---|
| 出典データセット | uspto-grants-2009_06 |
|---|
| ORD ID | ord-e258429c95244f978a203d3c7c534238 |
|---|
| 出典メモ | uspto-grants-2009_06 |
|---|