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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537729Generated: October 30, 2026

Isopropyl iodide → 4-Bromo-1-methoxy-2-[(propan-2-yl)oxy]benzene

https://huagongshe.com/reaction/537729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2-methoxyphenolHCID 142228—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-Bromo-1-methoxy-2-[(propan-2-yl)oxy]benzeneHCID 4673895282%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of 5-bromo-2-methoxyphenol (0.200 g, 1 mmol) in DMF (4 mL) was added potassium carbonate (0.209 g, 1.5 mmol) and isopropyliodide (120 μL, 1.2 mmol), the reaction mixture was stirred at room temperature (20° C.) for 3 h. After this time the crude reaction mixture was diluted with ethyl acetate (100 mL) and washed with water (2×100 mL). The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo to afford a yellow oil (200 mg, 0.81 mmol, 82%). No further purification was required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865699B2
Source datasetuspto-grants-2014_10
ORD IDord-95445d2b8c49402992f642be7715c4c5
Source noteuspto-grants-2014_10