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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 80761Erstellt: 23. Oktober 2026

Potassium Phosphate, Tribasic → 4-Cyclopropyl-2-hydroxybenzonitrile

https://huagongshe.com/de/reaction/80761

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium Phosphate, TribasicHCID 62657—
Edukt4-Bromo-2-hydroxybenzonitrileHCID 12966961—
EduktPotassium cyclopropyltrifluoroborateHCID 23697338—
KatalysatorBis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)HCID 11714597—
LösungsmittelTolueneHCID 1140—
LösungsmittelAmmonium chloride ethyl acetateHCID 86583716—
Produkt4-Cyclopropyl-2-hydroxybenzonitrileHCID 86690250—

Reaktionsbedingungen

Temperatur100 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846656B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-4c162c32089e4416946d0dfff84ac7b6
Quellennotizuspto-grants-2014_09