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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978626Generated: October 29, 2026

Sodium Iodide → HCID 21995720, compound

https://huagongshe.com/reaction/1978626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromoethyl ethyl etherHCID 61141—
Reactant4-bromo-N-ethylanilineHCID 11745656—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 21995720HCID 21995720—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of 4-bromo-N-ethylaniline (17.08 g) in DMF (100 ml) were added at room temperature potassium carbonate (17.1 g), sodium iodide (12.4 g) and 2-bromoethylethyl ether (10.2 ml), and the mixture was stirred at 90° C. for 24 hours. To the mixture were added 2-bromoethylethyl ether (5.0 ml), potassium carbonate (6.22 g) and sodium iodide (6.64 g), and the mixture was stirred for 2 days. To the mixture were added 2-bromoethylethyl ether (10.0 ml), potassium carbonate (17.1 g) and sodium iodide (12.4 g), and the mixture was stirred at 90° C. for 3 days. To the mixture was added water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried with magnesium sulfate. Under reduced pressure, the solvent was evaporated, and the residue was purified with silica gel column chromatography (ethyl acetate/hexane=1:9) to give yellow oil of 4-bromo-N-(2-propoxyethyl)-N-ethylaniline (18.11 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235771B1
Source datasetuspto-grants-2001_05
ORD IDord-848af3f2151c4109bed48fb138ebe349
Source noteuspto-grants-2001_05