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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445116Generated: October 25, 2026

Hydrochloric Acid → [4-[(3-Bromophenoxy)methyl]phenyl]boronic acid

https://huagongshe.com/reaction/445116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant3-BromophenolHCID 11563—
Reactant4-(Bromomethyl)phenylboronic acidHCID 2735593—
CatalystPotassium IodideHCID 4875—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product[4-[(3-Bromophenoxy)methyl]phenyl]boronic acidHCID 6797523450.8%

Reaction Steps

3-bromophenol (0.50 g) was dissolved in acetone, and to the resultant solution, potassium carbonate (1.49 g), potassium iodide (14 mg), and 4-bromomethylphenyl boronic acid (0.62 g) were added, followed by heating the resultant reaction mixture under reflux for 3 hours. The reaction mixture was left to be cooled down, and to the reaction mixture, water was added, and a 2M hydrochloric acid was added to adjust pH of the reaction mixture to 2 to 3, followed by extracting the reaction mixture with ethyl acetate. The organic phase was washed with saturated saline and was dried over anhydrous sodium sulfate. From the organic phase, the solvent was distilled off under reduced pressure, and the resultant residue was purified by silica gel column chromatography to obtain the subject compound (0.45 g) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476287B2
Source datasetuspto-grants-2013_07
ORD IDord-863fe1b89fa74fa7a3f641d3e8940456
Source noteuspto-grants-2013_07