HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 133546Erstellt: 24. Oktober 2026
Sodium Carbonate → N-(3-benzoyl-5-phenyl-thiophen-2-yl)-acetamide
https://huagongshe.com/de/reaction/133546
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | Phenylboronic Acid | HCID 66827 | — |
| Edukt | N-(3-benzoyl-5-bromo-thiophen-2-yl) acetamide | HCID 16640231 | — |
| Katalysator | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | N-(3-benzoyl-5-phenyl-thiophen-2-yl)-acetamide | HCID 68895390 | 88,6% |
Reaktionsschritte
A stirred solution of 0.448 g (1.38 mmol) of N-(3-benzoyl-5-bromo-thiophen-2-yl) acetamide in 20 ml toluene and 10 ml EtOH was degassed with argon. Tetrakis-(triphenylphosphine) palladium (0) (0.320 g, 0.27 mmol), phenyl boronic acid (0.194 g, 1.59 mmol) and 20 ml of an aqueous solution of Na2CO3 1N were added. The mixture was heated at 90° C. for 1 hour before cooling down to RT, filtered through Celite and concentrated. The mixture was extracted with ethyl acetate and aq. NaHCO3. The combined organic phases were dried over sodium sulfate and concentrated in vacuo. Flash chromatography (heptane/ethyl acetate 6:1) afforded 0.393 g (88%) N-(3-benzoyl-5-phenyl-thiophen-2-yl)-acetamide as a light yellow solid. ES-MS m/e (%): 322 (M+H+, 100).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07390903B2 |
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| Quelldatensatz | uspto-grants-2008_06 |
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| ORD ID | ord-05943aea103c471bbd9ee1e2aee9c135 |
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| Quellennotiz | uspto-grants-2008_06 |
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