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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784830Generated: October 30, 2026

Potassium Carbonate → 1-Bromo-3-iodo-5-(4-methoxy-benzyloxy)-benzene

https://huagongshe.com/reaction/1784830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Methyloxybenzyl chlorideHCID 69993—
Reactant3-Bromo-5-iodophenolHCID 22630182—
Catalyst4-Methyloxybenzyl chlorideHCID 69993—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Solventtert-Butyl methyl etherHCID 15413—
Product1-Bromo-3-iodo-5-(4-methoxy-benzyloxy)-benzeneHCID 5099402677.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Bromo-5-iodo-phenol (8.48 g, 28.37 mmol) was dissolved in DMF (50 mL) under dry argon and cooled to 0° C. Then potassium carbonate (3.92 g, 28.37 mmol) was added, followed by drop wise addition of 4-methoxybenzyl chloride (3.7 mL, 27.0 mmol). The mixture was slowly warmed to room temperature and stirred for 20 h. Additional 4-methoxybenzyl chloride (0.19 mL, 1.4 mmol) was added and the mixture was stirred for additional 24 h at room temperature. The reaction mixture was diluted with tert-butylmethyl ether (300 mL) and water (150 mL). The layers were separated and the aqueous one extracted with tert-butylmethyl ether (2×150 mL). The combined organics were washed with water and brine (150 mL), dried (Na2SO4) and concentrated to give the crude product which was purified by flash chromatography on silica gel (330 g, AcOEt/heptane 1:9). 1-Bromo-3-iodo-5-(4-methoxy-benzyloxy)-benzene (8.80 g, 59%, purity 80%, HPLC 220 nm) was obtained as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504401B2
Source datasetuspto-grants-2009_03
ORD IDord-c5c30b34a447446bb1f71cc9561ce8c5
Source noteuspto-grants-2009_03