Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988130Generated: November 4, 2026

Potassium Carbonate → HCID 178461418, compound

https://huagongshe.com/reaction/1988130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Cyanophenylboronic acidHCID 2734326—
ReactantHCID 178461415HCID 178461415—
CatalystHCID 178418476HCID 178418476—
SolventIsopropanolHCID 3776—
ProductHCID 178461418HCID 17846141833.5%

Reaction Steps

A solution of the product from Example 2A (100 mg, 0.34 mmol), 4-cyanophenyl boronic acid (65 mg, 0.44 mmol), dichlorobis(triphenylphosphine)palladium(II) (12 mg, 17 μmol) and potassium carbonate (120 mg, 0.85 mmol) under an atmosphere of nitrogen in isopropyl alcohol (8 mL) was heated at reflux for 5 hrs. Then, the reaction mixture was cooled to ambient temperature. The mixture was partitioned between ethyl acetate (25 mL) and H2O (10 mL). The organic layer was washed with brine, dried with magnesium sulfate, filtered, concentrated, and chromatographed on silica gel, eluting with 3% (9:1 MeOH:conc NH4OH) in dichloromethane to provide 36 mg of the title compound. 1H NMR (300 MHz, CD3OD) δ 1.21 (d, J=6 Hz, 3 H), 1.54 (m, 1 H), 1.84 (m, 2 H), 2.07 (m, 1 H), 2.18 (m, 2 H), 2.57 (m, 2 H), 2.71 (m, 2 H), 3.11 (m, 1 H), 3.27 (m, 2 H), 7.39 (d, J=9 Hz, 2 H), 7.64 (d, J=9 Hz, 2 H), 7.79 (s, 4 H); (DCl/NH3) m/z 317 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553964B2
Source datasetuspto-grants-2009_06
ORD IDord-bebcbf599d8949068272e808fd25c676
Source noteuspto-grants-2009_06