HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 269591Erstellt: 23. Oktober 2026
Hydrochloric Acid → 6''Fluoro-2-benzyloxy-[1,1':2',1'']terphenyl-3''-carboxylic acid
https://huagongshe.com/de/reaction/269591
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 3-Bromo-4-fluorobenzoic acid | HCID 70509 | — |
| Edukt | 2'-Benzyloxy-biphenyl-2-boronic acid | HCID 58730990 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 6''Fluoro-2-benzyloxy-[1,1':2',1'']terphenyl-3''-carboxylic acid | HCID 44581655 | — |
Reaktionsschritte
{2′-[(phenylmethyl)oxy]-2-biphenylyl}boronic acid (60 mg, 0.19 mmol) and 3-bromo-4-fluorobenzoic acid (69 mg, 0.31 mmol) were dissolved in 1:1 toluene:ethanol (6 ml) under nitrogen. Potassium carbonate (290 mg, 2.1 mmol) and tetrakis(triphenylphosphine)palladium(0) (23 mg, 0.019 mmol) were added and the mixture heated at 90° C. for 1 h. After cooling, the reaction mixture was poured into water, acidified with 1M HCl solution and extracted with ethyl acetate (15×2 ml), the combined organic layer were dried and evaporated. The residue was then purified on an SPE column using 40% of ethyl acetate in iso-hexane to give the title compound as white solid.
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-87b199b644b94a979230c2456be54945 |
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| Quellennotiz | uspto-grants-2008_11 |
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