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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450838Generated: October 31, 2026

Potassium Carbonate → omega-(2-Cyano-4-chlorophenoxy)-2-benzyloxy-acetophenone

https://huagongshe.com/reaction/450838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Chloro-2-hydroxybenzonitrileHCID 2777420—
Reactantomega-Bromo-2-benzyloxy-acetophenoneHCID 20153830—
SolventDimethylformamideHCID 6228—
Productomega-(2-Cyano-4-chlorophenoxy)-2-benzyloxy-acetophenoneHCID 68535637—

Reaction Steps

A suspension of potassium carbonate (0.06 g, 4.0 mmol), 4-chloro-2-cyanophenol (0.25 g, 1.6 mmol) and ω-bromo-2-benzyloxy-acetophenone (0.49 g, 1.6 mmol) in dry DMF (10 ml) is stirred at room temperature for 20 h. After evaporating the solvent under reduced pressure the residue is taken up in ethyl acetate. The solution is washed with water, dried over sodium sulfate and evaporated under reduced pressure. The residue is purified by silical gel column chromatography to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486996B2
Source datasetuspto-grants-2013_07
ORD IDord-d607c6706b354f9e9d4543951294f806
Source noteuspto-grants-2013_07