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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439768Generated: October 26, 2026

Potassium Carbonate → 4-(4-(Trifluoromethoxyphenoxy)phenoxy]butan-1-ol

https://huagongshe.com/reaction/439768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Bromo-4-(trifluoromethoxy)benzeneHCID 521008—
Reactant4-(4-Hydroxybutoxy)phenolHCID 22408055—
Product4-(4-(Trifluoromethoxyphenoxy)phenoxy]butan-1-olHCID 22407856—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 3.13 g of 4-(4-hydroxyphenoxy) butan-1-ol, 4.97 g of 4-(trifluoromethoxy)bromobenzene, and 4.75 g of K2CO3 are placed in a flask and flushed with N2 gas. To this are added 17 ml of pyridine and, after heating to 90° C.., 3.42 g of CuO. The reaction mixture is heated at reflux for 2 days, and then cooled and poured into an ice/3N HCl mixture. This mixture is extracted twice with ether; and after separating, the combined ether extracts are washed with saturated NaHCO3, followed by brine, and then dried over MgSO4. Filtration and evaporation yields an oily residue which is purified by flash chromatography on silica gel, using 2:1 hexane/EtOAc as eluant. After evaporation, 4-[4-(4-(trifluoromethoxyphenoxy)phenoxy]butan-1-ol is obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05516767
Source datasetuspto-grants-1996_05
ORD IDord-555f7a5d5c334d96a1b430a0a844bf1a
Source noteuspto-grants-1996_05