Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80761Generated: October 26, 2026

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

https://huagongshe.com/reaction/80761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-Bromo-2-hydroxybenzonitrileHCID 12966961—
ReactantPotassium cyclopropyltrifluoroborateHCID 23697338—
CatalystBis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)HCID 11714597—
SolventTolueneHCID 1140—
SolventAmmonium chloride ethyl acetateHCID 86583716—
Product4-Cyclopropyl-2-hydroxybenzonitrileHCID 86690250—

Reaction Conditions

Temperature100 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846656B2
Source datasetuspto-grants-2014_09
ORD IDord-4c162c32089e4416946d0dfff84ac7b6
Source noteuspto-grants-2014_09