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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839428Generated: October 25, 2026

3,4-Dichlorophenol → 2-(3,4-Dichlorophenoxy)-5-Fluoro-Benzonitrile

https://huagongshe.com/reaction/1839428

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DichlorophenolHCID 7258—
ReactantPotassium CarbonateHCID 11430—
Reactant2,5-DifluorobenzonitrileHCID 123558—
SolventDimethylformamideHCID 6228—
Product2-(3,4-Dichlorophenoxy)-5-Fluoro-BenzonitrileHCID 22019275—

Reaction Conditions

Temperature105 °C

Reaction Steps

A flame-dried flask containing N2 inlet and magnetic stirrer was charged with 2.9 g (18 mmol) of 3,4-dichlorophenol, 6.2 g (45 mmol) of potassium carbonate and 50 mL of anhydrous DMF. With stirring, 2.08 g (15 mmol) of 2,5-difluorobenzonitrile (Aldrich Chem. Co.) was added and the mixture was heated overnight at 105° C., cooled to room temperature and partitioned between water and EtOAc. The aqueous layer was reextracted with EtOAc and the combined organic layers were successively washed with 2N NaOH, water and saturated aqueous NaCl. After drying with MgSO4, the solvent was removed to give the title product as a light brown oil which slowly solidified, 3.5 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677378B2
Source datasetuspto-grants-2004_01
ORD IDord-d90a87fd6fda49678a2681745e2adb96
Source noteuspto-grants-2004_01