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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455322Generated: October 29, 2026

Potassium Iodide → 2-(2-Methyl-3-trifluoromethyl-phenoxy)-butyronitrile

https://huagongshe.com/reaction/455322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Methanesulfonyloxy)-butyronitrileHCID 15467691—
Reactant2-Methyl-3-(trifluoromethyl)phenolHCID 20111698—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Solventtert-Butyl methyl etherHCID 15413—
Product2-(2-Methyl-3-trifluoromethyl-phenoxy)-butyronitrileHCID 67017862—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-(methanesulfonyloxy)-butyronitrile (449 mg, 2.75 mmol), 2-methyl-3-trifluoromethylphenol (440 mg, 2.5 mmol), potassium carbonate (432 mg, 3.13 mmol) and potassium iodide (42 mg, 0.25 mmol) in acetonitrile (20 ml) was stirred overnight at 80° C. The mixture was shaken between tBuOMe and water, washed with NaCl (aq. satd) and the ethereal phase dried with MgSO4 and evaporated. The crude product was chromatographed on silica with EtOAc and hexane to give 2-(2-methyl-3-trifluoromethyl-phenoxy)-butyronitrile. 1H-NMR (CDCl3) 1.20 t, 3H; 2.15 dt, 2H; 2.36 s, 3H; 4.75, t, 2H; 7.17, d, 1H; 7.28, t, 1H; 7.37 d, 1H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497293B2
Source datasetuspto-grants-2013_07
ORD IDord-dbdf93172c13420ebc420505bb91342d
Source noteuspto-grants-2013_07