HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 547071Erstellt: 26. Oktober 2026
3-Ethyl-1-pentyn-3-ol → HCID 57443527, Verbindung
https://huagongshe.com/reaction/547071
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Ethyl-1-pentyn-3-ol | HCID 22698 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | (5-{4-[1-Ethyl-1-(3-methyl-4-trifluoromethanesulfonyloxy-phenyl)-propyl]-phenyl}-pyridin-3-yl)-acetic acid methyl ester | HCID 57709113 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Katalysator | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | HCID 57443527 | HCID 57443527 | 78,3% |
Reaktionsschritte
3-Ethyl-1-pentyn-3-ol (0.024 mL, 0.188 mmol), a [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II), dichloromethane complex (1:1) (10.6 mg, 0.013 mmol) and copper (I) iodide (2.5 mg, 0.013 mmol) were added to a solution of (5-{4-[1-ethyl-1-(3-methyl-4-trifluoromethanesulfonyloxy-phenyl)-propyl]-phenyl}-pyridin-3-yl)-acetic acid methyl ester (Example 144-(2); 67 mg, 0.125 mmol) in triethylamine (2 mL), and the mixture was stirred with microwave heating at 160° C. for three minutes. The reaction mixture was then poured into a saturated aqueous sodium bicarbonate solution, followed by extraction with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (hexane:ethyl acetate=1:1) to give the target compound (48.7 mg, 78%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07935688B2 |
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| Quelldatensatz | uspto-grants-2011_05 |
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| ORD ID | ord-a10a42cca6f44efcb0c862343fb0636b |
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| Quellennotiz | uspto-grants-2011_05 |
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