Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242947Generated: October 27, 2026

4-Bromophenol → 1-Bromo-4-[4-(trifluoromethoxy)phenoxy]benzene

https://huagongshe.com/reaction/2242947

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromophenolHCID 7808—
ReactantCesium carbonateHCID 10796—
Reactant2,2,6,6-Tetramethyl-3,5-heptanedioneHCID 70700—
Reactant1-Iodo-4-(trifluoromethoxy)benzeneHCID 2777294—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-Bromo-4-[4-(trifluoromethoxy)phenoxy]benzeneHCID 11530065—

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 4-bromophenol (0.173 g) in 4 mL of 1-methyl-2-pyrrolidone under argon atmosphere was treated with 4-(trifluoromethoxy)iodobenzene (0.313 mL), 2,2,6,6-tetramethylheptane-3,5-dione (0.046 mL) and caesium carbonate (0.652 g). The slurry was degassed by bubbling argon for 15 min and copper(I) chloride (0.099 g) was added. The reaction mixture was degassed by bubbling argon for 15 min, then heated to 100° C. under argon for 5 h. The reaction mixture was cooled to room temperature and added dropwise to 30 mL of tert-butyl-methyl-ether. The slurry was filtered and the solids washed with tert-butyl-methyl-ether (3×20 mL). The combined filtrates were washed subsequently with 1N NaOH (50 mL), water (50 mL), 2N HCl (50 mL), 1N HCl (50 mL), water (50 mL) and brine (50 mL). The resulting organic layer was dried over Na2SO4 and concentrated to give a crude product which was purified by column chromatography on silica gel eluting with hexane to afford 0.15 g of the title compound as a colourless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674808B2
Source datasetuspto-grants-2010_03
ORD IDord-9356f0c450c64a0caffad2e24111512c
Source noteuspto-grants-2010_03