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HRID 128808作成日:2026年10月24日

Trimethylsilylacetylene → 4-(Trimethylsilylethynyl)benzaldehyde

https://huagongshe.com/ja/reaction/128808

反応式

関与物質

役割名称HCID仕込み量
反応物TrimethylsilylacetyleneHCID 66111—
反応物4-BromobenzaldehydeHCID 70741—
生成物4-(Trimethylsilylethynyl)benzaldehydeHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05464865
出典データセットuspto-grants-1995_11
ORD IDord-95221e74419c4ae68a3338a64b69b627
出典メモuspto-grants-1995_11