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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397863Generated: October 26, 2026

Sodium Iodide → (2-(4-Bromophenoxy)ethyl)dimethylamine

https://huagongshe.com/reaction/397863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant4-BromophenolHCID 7808—
ReactantPotassium CarbonateHCID 11430—
ReactantN,N-Dimethylaminoethyl chloride hydrochlorideHCID 11636816—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product(2-(4-Bromophenoxy)ethyl)dimethylamineHCID 21387737.2%

Reaction Conditions

Temperature70 °C

Reaction Steps

4-Bromophenol (10.0 g, 57.8 mmol) and 2-dimethylaminoethyl chloride hydrochloride (8.33 g, 57.8 mmol) were dissolved in DMF (200 ml), and potassium carbonate (24.0 g, 173 mmol) and sodium iodide (0.87 g, 5.78 mmol) were added under ice-cooling. The mixture was stirred for 13 hr at room temperature and at 70° C. for 3 hr. Water (400 ml) was added to the reaction mixture and the mixture was extracted with chloroform (2×200 ml). The organic layer was washed successively with water (2×200 ml) and saturated brine (200 ml), dried over anhydrous magnesium sulfate and concentrated. The obtained residue was dissolved in 1N hydrochloric acid (100 ml) and washed with ethyl acetate (2×200 ml). Sodium hydroxide (4 g) was added to the aqueous layer to make the layer alkaline, and the mixture was extracted with chloroform (2×200 ml). The organic layer was dried over anhydrous magnesium sulfate and concentrated. Hexane was added to the obtained residue and insoluble matter was filtered off. The mother liquor was concentrated to give the title compound (5.25 g, 37%) as a transparent oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610729B1
Source datasetuspto-grants-2003_08
ORD IDord-31029c0552b14ee298a96c2a93e10fee
Source noteuspto-grants-2003_08