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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273384Generated: October 25, 2026

Potassium Iodide → 2-Bromo-5-(2-ethoxyethoxy)-1,3-dimethylbenzene

https://huagongshe.com/reaction/273384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantEthane, 1-chloro-2-ethoxy-HCID 12341—
Reactant4-Bromo-3,5-dimethylphenolHCID 81970—
SolventDimethylformamideHCID 6228—
Product2-Bromo-5-(2-ethoxyethoxy)-1,3-dimethylbenzeneHCID 2315769098%

Reaction Steps

To a solution of 4-bromo-3,5-dimethylphenol (12 g, 59.7 mmol), potassium iodide (1.5 g, 9.0 mmol) and potassium carbonate (9.9 g, 71.6 mmol) in N,N-dimethylformamide (80 mL) was added 2-chloroethyl ethyl ether (9.7 g, 89.3 mmol) at room temperature with stirring and the mixture was stirred at 70° C. for 2 days. The reaction mixture was cooled and concentrated under reduced pressure. The residue was partitioned between ethyl acetate and water. The organic layer was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=19/1) to give the title compound (15.9 g, yield 98%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456218B2
Source datasetuspto-grants-2008_11
ORD IDord-d36509fef7d647219d495960856c54a5
Source noteuspto-grants-2008_11