化工社化工社 化学情報印刷レポート · 研究参考用
Trimethylsilylacetylene → 4-(Trimethylsilylethynyl)benzaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trimethylsilylacetylene | HCID 66111 | — |
| 反応物 | 4-Bromobenzaldehyde | HCID 70741 | — |
| 生成物 | 4-(Trimethylsilylethynyl)benzaldehyde | HCID 2771643 | — |
反応手順
By the method of example 53(A), 4-bromobenzaldehyde is coupled with (trimethylsilyl)acetylene to provide 4-(2-(trimethylsilyl)ethynyl)benzaldehyde as a pale yellow solid after sublimation in vacuo. This material (5.8 g) is desilylated by stirring with potassium carbonate (0.4 g) in methanol (20 ml) for two hours. The solution is evaporated, and the product dissolved in methylene chloride, washed with water, dried, and concentrated to provide 4-ethynylbenzaldehyde as a yellow solid (3.45 g, 90%). By the Wittig reaction of example 1(A), this is chain-extended to provide 1-ethynyl-4-(2-methoxyethenyl)benzene, obtained as a colorless oil after distillation in vacuo (3.10 g, 77%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05464865 |
| 出典データセット | uspto-grants-1995_11 |
| ORD ID | ord-95221e74419c4ae68a3338a64b69b627 |
| 出典メモ | uspto-grants-1995_11 |