HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1098749Erstellt: 23. Oktober 2026
Triethylamine → N-[1-(3-Pentafluoroethyl-phenyl)-vinyl]-acetamide
https://huagongshe.com/de/reaction/1098749
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | N-Vinylacetamide | HCID 78875 | — |
| Edukt | Phosphine, (1-methylethylidene)bis[diphenyl- | HCID 12091099 | — |
| Edukt | Trifluoro-methanesulfonic acid 3-pentafluoroethyl-phenyl ester | HCID 59506217 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-[1-(3-Pentafluoroethyl-phenyl)-vinyl]-acetamide | HCID 59506293 | — |
Reaktionsschritte
To a solution of the crude product of step 1 (0.75 g, 2.2 mmol) in DMF (10 ml) was added N-vinylacetamide (0.37 g, 4.36 mmol), triethylamine (243 mg, 0.33 ml, 2.40 mmol), palladium acetate (20 mg, 4 mol %) and bis(diphenylphosphino)propane (40 mg, 0.1 mmol). The reaction mixture was heated for 30 min at 130° C. using microwaves. The red solution was diluted and washed with hydrochloric acid (1M, 2×15 ml) and sodium hydrogen carbonate (saturated, 20 ml). The organic phase was dried over sodium sulphate and evaporated. Purification of the crude product by silica gel chromatography using ethyl acetate/n-heptane (2:1) gave the desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08143242B2 |
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| Quelldatensatz | uspto-grants-2012_03 |
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| ORD ID | ord-952ca0b47f1a49ef9fa38068bfe476a6 |
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| Quellennotiz | uspto-grants-2012_03 |
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