HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 418855Erstellt: 25. Oktober 2026
2-Bromobenzaldehyde → 2-((4-Methoxyphenyl)ethynyl)benzaldehyde
https://huagongshe.com/reaction/418855
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Bromobenzaldehyde | HCID 81129 | — |
| Edukt | 1-Ethynyl-4-methoxybenzene | HCID 251020 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | 2-((4-Methoxyphenyl)ethynyl)benzaldehyde | HCID 12997240 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08093273B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-42f87fc1d9d34de1a850a74154217349 |
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| Quellennotiz | uspto-grants-2012_01 |
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