HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 269543Erstellt: 26. Oktober 2026
Potassium Carbonate → 2-Benzyloxy-[1,1';2',1'']terphenyl-4''-sulfonic acid (1-phenyl-methanoyl)-amide
https://huagongshe.com/reaction/269543
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | N-(4-bromobenzenesulfonyl)benzamide | HCID 766162 | — |
| Edukt | Toluene ethanol | HCID 21863594 | — |
| Edukt | 2'-Benzyloxy-biphenyl-2-boronic acid | HCID 58730990 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-Benzyloxy-[1,1';2',1'']terphenyl-4''-sulfonic acid (1-phenyl-methanoyl)-amide | HCID 10029631 | — |
Reaktionsschritte
A mixture of 2′-benzyloxy-biphenyl-2-boronic acid (100 mg, 0.33 mmol), 4-bromo-N-(1-phenyl-methanoyl)-benzenesulfonamide (95 mg, 0.28 mmol), potassium carbonate (309 mg, 2.24 mmol), and tetrakis(triphenylphosphine)palladium(0) (38 mg, 0.033 mmol) in 1:1 toluene/ethanol (5 ml) was stirred and heated at 90° C. under nitrogen for 16 hours. After cooling the mixture was diluted with ethyl acetate and water. The organic phase was dried and evaporated. The residue was chromatographed eluting with ethyl acetate/iso-hexane (1:4-1:1) to give the title compound as a colourless solid. (40 mg 23%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07446222B2 |
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| Quelldatensatz | uspto-grants-2008_11 |
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| ORD ID | ord-f223f0c3235c49968b831589534a2cf9 |
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| Quellennotiz | uspto-grants-2008_11 |
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