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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254970Generated: October 25, 2026

Potassium Carbonate → 2-(2-Chloro-3-trifluoromethyl-phenoxy)-butyronitrile

https://huagongshe.com/reaction/1254970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl methyl etherHCID 15413—
Reactant2-Chloro-3-(trifluoromethyl)phenolHCID 2736601—
Reactant2-(Methanesulfonyloxy)-butyronitrileHCID 15467691—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-(2-Chloro-3-trifluoromethyl-phenoxy)-butyronitrileHCID 68735070—

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 2-(methanesulfonyloxy)-butyronitrile (204 mg, 1.25 mmol) (prepared following Marco et. al., Tetrahedron, 2000, 56, 2525-31) 2-chloro-3-trifluoromethylphenol (196 mg, 1.0 mmol) and potassium carbonate (172 mg, 1.25 mmol) in acetonitrile (5 ml) was stirred for 1 hour at 95° C. The mixture was shaken between tBuOMe and water and the ethereal phase dried with Na2SO4, filtered over a silicagel pad and evaporated to give as yellowish oil 2-(2-chloro-3-trifluoromethyl-phenoxy)-butyronitrile; 1H-NMR (CDCl3): 1.27 t, 3H, 2.20 m, 2H, 2.40 s, 3H, 4.78 t, 1H, 7.34, d, 1H; 7.39, t, 1H, 7.48 d, 1H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455663B2
Source datasetuspto-grants-2013_06
ORD IDord-2a187544f3ea4e37bd4d380196138f44
Source noteuspto-grants-2013_06