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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 418855Erstellt: 25. Oktober 2026

2-Bromobenzaldehyde → 2-((4-Methoxyphenyl)ethynyl)benzaldehyde

https://huagongshe.com/reaction/418855

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-BromobenzaldehydeHCID 81129—
Edukt1-Ethynyl-4-methoxybenzeneHCID 251020—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelTriethylamineHCID 8471—
Produkt2-((4-Methoxyphenyl)ethynyl)benzaldehydeHCID 1299724089%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

To a solution of 2-bromobenzaldehyde (1.85 g, 10 mmol) and 4-methoxyphenyl acetylene (1.58 g, 12 mmol) in 40 mL of triethylamine were added dichlorobis(triphenylphosphine) palladium(II) (140 mg, 2 mol %) and copper(I) iodide (20 mg, 1 mol %). The reaction mixture was heated at 50° C. under nitrogen for 3 h. The reaction mixture was cooled to room temperature and the ammonium salt was removed by filtration. The filtrate was concentrated under reduced pressure. Purification of the crude compound by column chromatography (SilicaGel 230-400 mesh; 10% ethyl acetate in hexanes as eluent) afforded of 2-(4-methoxy phenylethynyl)benzaldehyde (2.1 g, 89%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093273B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-42f87fc1d9d34de1a850a74154217349
Quellennotizuspto-grants-2012_01