HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744514Generated: October 31, 2026
Potassium Iodide → 2-Bromo-1-(2-methylpropoxy)-4-nitrobenzene
https://huagongshe.com/reaction/1744514
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | HCID 13049719 | HCID 13049719 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Bromo-1-(2-methylpropoxy)-4-nitrobenzene | HCID 13749790 | 87% |
Reaction Steps
Subsequently, a catalytic amount of potassium iodide was added to 4-isobutoxynitrobenzene (203 g) and the mixture was heated to 60° C. Bromine (183 g) was added dropwise over 3 h. The mixture was stirred further for 1 h. The reaction mixture was poured into water and extracted with toluene. The organic layer was washed with aqueous sodium sulfite solution and dried over anhydrous magnesium sulfate, after which the solvent was evaporated under reduced pressure. The obtained oily substance was distilled under reduced pressure to give 2-isobutoxy-5-nitrobromobenzene (248 g), boiling point: 135–140° C./0.25 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07015218B1 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-b38bfa3662334ae3b68aca53b2915fed |
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| Source note | uspto-grants-2006_03 |
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