HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978741Generated: October 25, 2026
Sodium Iodide → 1-Bromo-3-ethoxy-4-(2-ethoxyethoxy)benzene
https://huagongshe.com/reaction/1978741
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromoethyl ethyl ether | HCID 61141 | — |
| Reactant | 4-Bromo-2-ethoxyphenol | HCID 21877541 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Bromo-3-ethoxy-4-(2-ethoxyethoxy)benzene | HCID 21995818 | — |
Reaction Steps
A suspension of 4-bromo-2-ethoxyphenol (8 g), bromoethylethyl ether (5 ml), sodium iodide (5.5 g) and potassium carbonate (10.2 g) in DMF (10 ml) was stirred under nitrogen atmosphere at 90° C. overnight. The solvent was evaporated, and to the residue was added water. The mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried with anhydrous magnesium sulfate. The solvent was evaporated, and the residue was distilled under reduced pressure to give 1-bromo-3-ethoxy-4-(2-ethoxyethoxy)benzene (8.1 g) as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06235771B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-634e959b69c5429c9d5a0e10160dfb97 |
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| Source note | uspto-grants-2001_05 |
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