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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822327Generated: October 25, 2026

Phenol → 2-Phenoxy-3-trifluoromethyl-anisole

https://huagongshe.com/reaction/1822327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoro-1-methoxy-3-(trifluoromethyl)benzeneHCID 2774768—
SolventDimethyl SulfoxideHCID 679—
Product2-Phenoxy-3-trifluoromethyl-anisoleHCID 6907610053%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 2-fluoro-3-methoxybenzotrifluoride (4.76 g, 24.5 mmol), phenol (2.30 g, 24.4 mmol) and 325 mesh potassium carbonate (4.07 g, 29.4 mmol) in dry DMSO (50 mL) is heated to 130° C. and stirred 17 hours under N2. The reaction filtered to remove the solids, and the filtrate is acidified with 1 N HCl. The mixture is then diluted with water and extracted with Et2O. The organic layer is dried (Na2SO4) and the solvent is removed in vacuo to afford crude product that is absorbed on silica gel and purified by flash chromatography using 12/1 hexanes/ethyl acetate to afford 3.47 g (53%) of 2-phenoxy-3-trifluoromethyl-anisole (Rf=0.30 (4/1 hexanes/EtOAc) that is contaminated with starting 2-fluoro-1-methoxy-3-trifluoromethyl-benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608639B2
Source datasetuspto-grants-2009_10
ORD IDord-326347f9d7c24688a96f2c9a8ef4c32a
Source noteuspto-grants-2009_10