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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642237Generated: October 31, 2026

2,4-Dichlorophenol → 2-(2,4-Dichlorophenoxy)benzonitrile

https://huagongshe.com/reaction/1642237

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichlorophenolHCID 8449—
ReactantPotassium CarbonateHCID 11430—
Reactant2-FluorobenzonitrileHCID 67855—
SolventDimethylformamideHCID 6228—
Product2-(2,4-Dichlorophenoxy)benzonitrileHCID 2777020—

Reaction Steps

AMR01045 A mixture of 2,4-dichlorophenol (2.00 g, 12.27 mmol), 2-fluorobenzonitrile (1.49 g, 12.27 mmol) and potassium carbonate (1.7 g, 12.27 mmol) in DMF (10 mL) was stirred under reflux for 1.5 h. After removal of DMF, the residue was dissolved in DCM and washed with NaOH (5%, 3×20 mL) and brine. The organic layer was dried (MgSO4), filtered and evaporated and 2-(2,4-dichlorophenoxy)benzonitrile was obtained as an oil (2.73 g, 84%), which was used in the next step without further purification. Rf: 0.64 (DCM) 1H NMR (300 MHz, CDCl3) δ 6.73 (1H, dd, J=8.4 Hz), 7.13 (1H, d, J=8.7 Hz), 7.22 (1H, td, J=8.7, 1.0 Hz), 7.35 (1H, dd, J=8.7, 2.4 Hz), 7.56 (1H, d, J=2.4 Hz) and 7.73 (1H, dd, J=7.5, 2.7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119627B2
Source datasetuspto-grants-2012_02
ORD IDord-46a8b4528f2541b48c9d17f872d16241
Source noteuspto-grants-2012_02