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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 128808Erstellt: 23. Oktober 2026

Trimethylsilylacetylene → 4-(Trimethylsilylethynyl)benzaldehyde

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilylacetyleneHCID 66111—
Edukt4-BromobenzaldehydeHCID 70741—
Produkt4-(Trimethylsilylethynyl)benzaldehydeHCID 2771643—

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05464865
Quelldatensatzuspto-grants-1995_11
ORD IDord-95221e74419c4ae68a3338a64b69b627
Quellennotizuspto-grants-1995_11