HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 243875Erstellt: 26. Oktober 2026
Sodium Bicarbonate → 3-fluoro-2-(1H-pyrazol-5-yl)benzonitrile
https://huagongshe.com/reaction/243875
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 2-Bromo-3-fluorobenzonitrile | HCID 2783393 | — |
| Edukt | 1H-Pyrazole-5-boronic acid | HCID 11251979 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | 1,2-Dimethoxyethane | HCID 8071 | — |
| Produkt | 3-fluoro-2-(1H-pyrazol-5-yl)benzonitrile | HCID 67116928 | 20,7% |
Reaktionsschritte
2-Bromo-3-fluorobenzonitrile (1.0 g, 5.0 mmol) and (1H-pyrazol-5-yl)boronic acid (647 mg, 4.6 mmol) were combined and dissolved in degassed DME (15 mL) then treated with NaHCO3 (1260 mg, 8.4 mmol) in water and the reaction purged with bubbling N2 for 5 minutes. The reaction was treated with Pd(PPh3)4 (288 mg, 0.2 mmol) and then purged with bubbling for 5 minutes in a sealed vessel and then heated to reflux for 2 h. The reaction was then cooled to 23° C. filtered and the solids were rinsed with EtOAc and the layers separated. The organic layers were combined, dried and concentrated under reduced pressure. Chromatography (0-30% ethyl acatate/hexanes) afforded 3-fluoro-2-(1H-pyrazol-5-yl)benzonitrile (178 mg, 19%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08653263B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-a08601227d3d4cc4a757065d38125524 |
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| Quellennotiz | uspto-grants-2014_02 |
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