HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1752Erstellt: 23. Oktober 2026
Diethyl Ether → t-Butyl 3-{6-hydroxymethyl-3-[8(4-methoxyphenyl)octyloxy]pyridin-2-yl}propenoate
https://huagongshe.com/de/reaction/1752
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | tert-Butyl acrylate | HCID 15458 | — |
| Edukt | Potassium Acetate | HCID 517044 | — |
| Edukt | 2-Bromo-6-hydroxymethyl-[8(4-methoxyphenyl)octyloxy]pyridine | HCID 19692711 | — |
| Katalysator | Tetrabutylammonium Iodide | HCID 67553 | — |
| Katalysator | HCID 178418476 | HCID 178418476 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | t-Butyl 3-{6-hydroxymethyl-3-[8(4-methoxyphenyl)octyloxy]pyridin-2-yl}propenoate | HCID 54231524 | — |
Reaktionsschritte
To a solution of 2-bromo-6-hydroxymethyl-[8(4-methoxyphenyl)octyloxy]pyridine (5.00 g, 11.8 mmol) in DMF (22.8 ml) and water (1.2 ml) were added potassium acetate (3.00 g, 30.6 mmol), tetra-n-butylammonium iodide (4.36 g, 11.8 mmol), bis(triphenylphosphine)palladium dichloride (0.33 g, 0.47 mmol) and t-butyl acrylate (6.16 g, 48 mmol). The mixture was placed under nitrogen and stirred and heated at 120° C. for 45 min. The mixture was cooled and added to water (250 ml). The product was extracted into ethyl acetate (2×60 ml). The combined extracts were washed with water (100 ml), 5% sodium chloride solution (2×100 ml), then dried and evaporated. The product was obtained by flash column chromatography using silica and 10% ether in dichloromethane. Yield 4.29 g, 77%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05726315 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-518c5ae80b704ac1999ffc9853c652ad |
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| Quellennotiz | uspto-grants-1998_03 |
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