HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 80761Erstellt: 23. Oktober 2026
Potassium Phosphate, Tribasic → 4-Cyclopropyl-2-hydroxybenzonitrile
https://huagongshe.com/de/reaction/80761
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Edukt | 4-Bromo-2-hydroxybenzonitrile | HCID 12966961 | — |
| Edukt | Potassium cyclopropyltrifluoroborate | HCID 23697338 | — |
| Katalysator | Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) | HCID 11714597 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Ammonium chloride ethyl acetate | HCID 86583716 | — |
| Produkt | 4-Cyclopropyl-2-hydroxybenzonitrile | HCID 86690250 | — |
Reaktionsschritte
A solution of 4-bromo-2-hydroxybenzonitrile (1 g, 5.05 mmol), potassium cyclopropyltrifluoroborate (1.495 g, 10.10 mmol), K3PO4 (5.05 ml, 15.15 mmol) and PdCl2(Amphos)2 (0.358 g, 0.505 mmol) in toluene (25 mL) was allowed to stir at 100° C. under nitrogen overnight. The mixture was then cooled to room temperature, diluted with EtOAc/NH4Cl(aq), and filtered through a pad of Celite. The organic layer was seperated, dried over Na2SO4, filtered and concentrated. The residue was purified by FCC (0-50% EtOAc/heptane) to provide 4-cyclopropyl-2-hydroxybenzonitrile, 1H NMR (400 MHz, CH2Cl2) δ 12.17 (br. s., 1H), 7.23 (d, J=8.34 Hz, 1H), 6.51-6.58 (m, 2H), 1.82 (tt, J=5.02, 8.37 Hz, 1H), 0.94-1.00 (m, 2H), 0.68-0.73 (m, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08846656B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-4c162c32089e4416946d0dfff84ac7b6 |
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| Quellennotiz | uspto-grants-2014_09 |
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